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Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12617001474347
Ethics application status
Approved
Date submitted
8/03/2017
Date registered
19/10/2017
Date last updated
24/09/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Pancreatic cancer: Understanding Routine Practice and Lifting End Results (PURPLE). A Prospective Pancreatic Cancer Clinical Registry
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Scientific title
Pancreatic cancer: Understanding Routine Practice and Lifting End Results (PURPLE). A Prospective Pancreatic Cancer Clinical Registry
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Secondary ID [1]
291388
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Nil Known
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Universal Trial Number (UTN)
U1111-1193-9819
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Trial acronym
PURPLE Registry
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pancreatic Cancer
302408
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Newly diagnosed Pancreatic Cancer
302409
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Metastatic Pancreatic Cancer
302410
0
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Condition category
Condition code
Cancer
301982
301982
0
0
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Pancreatic
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
3
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Target follow-up type
Years
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Description of intervention(s) / exposure
The following end-points will be evaluated in this study: Time to progression from primary diagnosis (TTP). Progression-free survival (PFS). Overall survival (OS). This project is a multi-centre, prospective cohort study that will aim to enrol 800 patients at participating sites. It involves collection of data into the PURPLE registry, linkage and analysis of data via a WEHI developed database. Comprehensive clinicopathological data will be collected, start and stop dates for all systemic therapies will be captured as well as treatment response data for each therapy used, the reason for any change in treatment, and the date of disease progression. Data related to any resection of primary and or metastatic disease will be collected.
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Intervention code [1]
297427
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
301756
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Time to progression from primary diagnosis (TTP) will be assessed by treating doctor for up to 3 years at clinician's discretion using MRI scan, CT scan or PET scan or PET-CT scan.
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Assessment method [1]
301756
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Timepoint [1]
301756
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Assessed once per year for three years from enrolment. will be assessed by treating doctor for up to 3 years at clinician's discretion using MRI scan, CT scan or PET scan or PET-CT scan.
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Primary outcome [2]
303414
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Progression-free survival (PFS)will be assessed by treating doctor for up to 3 years at clinician's discretion using MRI scan, CT scan or PET scan or PET-CT scan.
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Assessment method [2]
303414
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Timepoint [2]
303414
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Once at the starts pf the study and at various timepoints for up to 3 years at clinician's discretion , will be assessed by MRI scan, CT scan or PET scan or PET-CT scan.
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Primary outcome [3]
303461
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Overall survival (OS will be assessed by will be assessed by treating doctor for up to 3 years at clinician's discretion using MRI scan, CT scan or PET scan or PET-CT scan.
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Assessment method [3]
303461
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Timepoint [3]
303461
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At the start of the study and during regular clinic visits at the hospital will be assessed by MRI scan, CT scan or PET scan or PET-CT scan.
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Secondary outcome [1]
332536
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To determine the impact of age, on clinicians’ treatment recommendations looking at patient medical records.
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Assessment method [1]
332536
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Timepoint [1]
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Assessed once per year for three years from enrolment.
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Secondary outcome [2]
333765
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To determine the impact of co morbidity, on clinicians’ treatment recommendations looking at patient medical records.
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Assessment method [2]
333765
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Timepoint [2]
333765
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Assessed once per year for three years from enrolment.
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Secondary outcome [3]
333766
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To identify factors influencing the choice of FOLFOXIRI vs. Abraxane/ Gemcitabine in the first line setting by reviewing patient medical records.
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Assessment method [3]
333766
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Timepoint [3]
333766
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Assessed once per year for three years from enrolment.
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Secondary outcome [4]
333767
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To obtain data on the most common chemotherapy regimens prescribed in the first-line setting by reviewing patient medical records
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Assessment method [4]
333767
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Timepoint [4]
333767
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Assessed once per year for three years from enrolment.
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Secondary outcome [5]
333769
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To analyze the range of second-line chemotherapy choices for patients by looking at Medical records. .
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Assessment method [5]
333769
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Timepoint [5]
333769
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Assessed once per year for three years from enrolment.
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Secondary outcome [6]
333770
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To determine the rate at which adverse events that could be attributed to the treatment regimen occur in routine clinical practice by reviewing medical records
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Assessment method [6]
333770
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Timepoint [6]
333770
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Assessed once per year for three years from enrolment.
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Secondary outcome [7]
333771
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To estimate the progression free survival first. and second-line advanced unresectable or metastatic pancreatic cancer patients. By reviewing medical records.
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Assessment method [7]
333771
0
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Timepoint [7]
333771
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Assessed once per year for three years from enrolment.
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Secondary outcome [8]
333772
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To determine the number of patients that receive any treatment and for patients that are not treated the reasons that chemotherapy was not given by reviewing medical records.
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Assessment method [8]
333772
0
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Timepoint [8]
333772
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Assessed once per year for three years from enrolment.
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Secondary outcome [9]
333773
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To determine the range of chemotherapy choices (single or multiple options) given to patients by reviewing patient medical records
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Assessment method [9]
333773
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Timepoint [9]
333773
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Assessed once per year for three years from enrolment.
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Secondary outcome [10]
333774
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To determine the duration of treatment in the first and second line setting by reviewing patient medical records.
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Assessment method [10]
333774
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Timepoint [10]
333774
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Assessed once per year for three years from enrolment.
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Secondary outcome [11]
333775
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To determine the number of patients undergoing potentially curative resection of distant metastases or alternative interventions by reviewing patient medical records
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Assessment method [11]
333775
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Timepoint [11]
333775
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Assessed once per year for three years from enrolment.
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Secondary outcome [12]
333819
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looking at overall survival of first and second-line advanced unresectable or metastatic pancreatic cancer patients.
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Assessment method [12]
333819
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Timepoint [12]
333819
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Assessed once per year for three years from enrolment.
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Eligibility
Key inclusion criteria
Patients with newly diagnosed pancreatic cancer, with or without metastatic disease
b) Histologically or cytologically confirmed diagnosis of pancreatic cancer
c) Patients aged 18 years or above with any ECOG performance status with pancreatic cancer
d) Patients who are yet to receive treatment
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients that do not have a new diagnosis of pancreatic cancer. .
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
It is anticipated that a sample size of 800 is sufficient to achieve the aim of this study, and to achieve preliminary insights into variation in practice and outcomes across sites. In order to compare clinical outcomes across different subgroups, Kaplan-Meier survival curves will be defined from survival data and constructed using SAS (registered trademark) software. The stratified log rank test will be used to compare survival curves between different groups of participants. P-values of 0.05 will be considered significant. Due to the non-randomised nature of such comparisons propensity score techniques will be used to balance comparison groups according to baseline factors.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
15/02/2017
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Date of last participant enrolment
Anticipated
31/07/2020
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Actual
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Date of last data collection
Anticipated
31/07/2023
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Actual
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Sample size
Target
800
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Accrual to date
740
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,QLD,SA,TAS,WA,VIC
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Recruitment hospital [1]
7611
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Royal Melbourne Hospital - City campus - Parkville
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Recruitment hospital [2]
7612
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Western Hospital - Footscray - Footscray
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Recruitment hospital [3]
7613
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Peter MacCallum Cancer Centre - Melbourne
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Recruitment hospital [4]
7614
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Box Hill Hospital - Box Hill
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Recruitment hospital [5]
7615
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Cabrini Hospital - Malvern - Malvern
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Recruitment hospital [6]
7616
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Epworth Richmond - Richmond
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Recruitment hospital [7]
7617
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [8]
7618
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Monash Medical Centre - Moorabbin campus - East Bentleigh
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Recruitment hospital [9]
7619
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St Vincent's Hospital (Melbourne) Ltd - Fitzroy
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Recruitment hospital [10]
7620
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [11]
7621
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The Alfred - Prahran
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Recruitment hospital [12]
7622
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Ballarat Health Services (Base Hospital) - Ballarat Central
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Recruitment hospital [13]
7623
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Goulburn Base Hospital - Goulburn
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Recruitment hospital [14]
7624
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The Northern Hospital - Epping
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Recruitment hospital [15]
7625
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Barwon Health - Geelong Hospital campus - Geelong
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Recruitment hospital [16]
7626
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Royal Brisbane & Womens Hospital - Herston
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Recruitment hospital [17]
7627
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Gold Coast University Hospital - Southport
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Recruitment hospital [18]
7628
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The Canberra Hospital - Garran
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Recruitment hospital [19]
7629
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The Queen Elizabeth Hospital - Woodville
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Recruitment hospital [20]
7630
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Flinders Medical Centre - Bedford Park
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Recruitment hospital [21]
7631
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Prince of Wales Hospital - Randwick
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Recruitment hospital [22]
7632
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Liverpool Hospital - Liverpool
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Recruitment hospital [23]
7633
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Campbelltown Hospital - Campbelltown
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Recruitment hospital [24]
7634
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Southern Highlands Private Hospital - Bowral
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Recruitment hospital [25]
7635
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Westmead Hospital - Westmead
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Recruitment hospital [26]
7636
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Calvary Mater Newcastle - Waratah
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Recruitment hospital [27]
7637
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John Hunter Hospital - New Lambton
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Recruitment hospital [28]
7638
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The Chris O’Brien Lifehouse - Camperdown
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Recruitment hospital [29]
7639
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St John of God Hospital, Subiaco - Subiaco
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Recruitment hospital [30]
7640
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Royal Hobart Hospital - Hobart
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Recruitment hospital [31]
7641
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Fiona Stanley Hospital - Murdoch
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Recruitment hospital [32]
7642
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Wellington Health Service - Wellington
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Recruitment postcode(s) [1]
15514
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3000 - Melbourne
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Recruitment postcode(s) [2]
15515
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3050 - Parkville
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Recruitment postcode(s) [3]
15516
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3011 - Footscray
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Recruitment postcode(s) [4]
15517
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3128 - Box Hill
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Recruitment postcode(s) [5]
15518
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3144 - Malvern
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Recruitment postcode(s) [6]
15519
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3121 - Richmond
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Recruitment postcode(s) [7]
15520
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3168 - Clayton
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Recruitment postcode(s) [8]
15521
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3165 - East Bentleigh
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Recruitment postcode(s) [9]
15522
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3065 - Fitzroy
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Recruitment postcode(s) [10]
15523
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3084 - Heidelberg
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Recruitment postcode(s) [11]
15524
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3004 - Prahran
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Recruitment postcode(s) [12]
15525
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3350 - Ballarat Central
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Recruitment postcode(s) [13]
15526
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2580 - Goulburn
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Recruitment postcode(s) [14]
15527
0
3076 - Epping
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Recruitment postcode(s) [15]
15528
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3220 - Geelong
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Recruitment postcode(s) [16]
15529
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4029 - Herston
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Recruitment postcode(s) [17]
15530
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4215 - Southport
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Recruitment postcode(s) [18]
15531
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2605 - Garran
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Recruitment postcode(s) [19]
15532
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5011 - Woodville
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Recruitment postcode(s) [20]
15533
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5042 - Bedford Park
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Recruitment postcode(s) [21]
15534
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2031 - Randwick
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Recruitment postcode(s) [22]
15535
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2170 - Liverpool
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Recruitment postcode(s) [23]
15536
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2560 - Campbelltown
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Recruitment postcode(s) [24]
15537
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2576 - Bowral
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Recruitment postcode(s) [25]
15538
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2145 - Westmead
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Recruitment postcode(s) [26]
15539
0
2298 - Waratah
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Recruitment postcode(s) [27]
15540
0
2305 - New Lambton
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Recruitment postcode(s) [28]
15541
0
2050 - Camperdown
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Recruitment postcode(s) [29]
15542
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6008 - Subiaco
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Recruitment postcode(s) [30]
15543
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7000 - Hobart
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Recruitment postcode(s) [31]
15544
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6150 - Murdoch
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Recruitment postcode(s) [32]
15545
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2820 - Wellington
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Recruitment outside Australia
Country [1]
8720
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Singapore
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State/province [1]
8720
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Singapore
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Country [2]
8721
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United Kingdom
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State/province [2]
8721
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London
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Country [3]
8722
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Hong Kong
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State/province [3]
8722
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hong kong
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Funding & Sponsors
Funding source category [1]
295861
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Other
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Name [1]
295861
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Hemstritch Philanthropic fund
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Address [1]
295861
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Walter and Eliza Hall Institute
1G Royal Parade
Parkville 3050 Victoria Australia
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Country [1]
295861
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Australia
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Primary sponsor type
Other Collaborative groups
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Name
Walter & Eliza Hall Institute
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Address
1G Royal Parade
Parkville 3050 Victoria Australia
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Country
Australia
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Secondary sponsor category [1]
294726
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None
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Name [1]
294726
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Address [1]
294726
0
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Country [1]
294726
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
297144
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MELBOURNE HEALTH HUMAN RESEARCH ETHICS COMMITTEE
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Ethics committee address [1]
297144
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Office for Research The Royal Melbourne Hospital Level 2 South West 300 Grattan Street Parkville VIC 3050 Victoria Australia
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Ethics committee country [1]
297144
0
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Date submitted for ethics approval [1]
297144
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27/07/2016
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Approval date [1]
297144
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30/08/2016
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Ethics approval number [1]
297144
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2016.200
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Summary
Brief summary
This project is non-interventional registry of the treatment and outcomes of patients with pancreatic cancer managed at hospitals enrolled to participate in Australia. Who is it for? You may be eligible to join this study if you are aged 18 years or above and have been newly diagnosed with pancreatic cancer (with or without metastatic disease) , with any ECOG performance status and are yet to receive treatment. Study details This registry will capture data on presentation and the disease course of pancreatic cancer, surgical interventions for primary and metastatic disease, prescription of systemic therapies, and information regarding multi-disciplinary management and outcomes of this disease in the routine clinical practice setting. This project will collect clinical data using the already established data collection and analysis resources built up over the last 15 years in the Systems Biology & Personalised Medicine Division of the Walter & Eliza Hall Institute of medical research (WEHI). This protocol aims to enrol at least 800 eligible patients over 10 years. Findings from analyses that occur as part of this project are anticipated to improve our understanding of the presentation, clinical course and management of pancreatic cancer in Australia and other participating countries.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
73118
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A/Prof Peter Gibbs
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Address
73118
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The Walter and Eliza Hall Institute of Medical Research
1G Royal Parade, Parkville VIC 3052 Australia
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Country
73118
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Australia
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Phone
73118
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+61 3 93424269
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Fax
73118
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+61 3 93452317
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Email
73118
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[email protected]
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Contact person for public queries
Name
73119
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Belinda Lee
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Address
73119
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The Walter and Eliza Hall Institute of Medical Research
1G Royal Parade, Parkville VIC 3052 Australia
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Country
73119
0
Australia
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Phone
73119
0
+61 3 9845 2853
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Fax
73119
0
+61 3 93452317
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Email
73119
0
[email protected]
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Contact person for scientific queries
Name
73120
0
Belinda Lee
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Address
73120
0
The Walter and Eliza Hall Institute of Medical Research
1G Royal Parade, Parkville VIC 3052 Australia
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Country
73120
0
Australia
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Phone
73120
0
+61 3 9845 2853
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Fax
73120
0
+61 3 93452317
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Email
73120
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Use and outcomes of chemotherapy for metastatic pancreatic cancer in Australia.
2022
https://dx.doi.org/10.1111/imj.15094
Embase
Use and outcomes from neoadjuvant chemotherapy in borderline resectable pancreatic ductal adenocarcinoma in an Australasian population.
2023
https://dx.doi.org/10.1111/ajco.13807
N.B. These documents automatically identified may not have been verified by the study sponsor.
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