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Trial registered on ANZCTR
Registration number
ACTRN12611000593932
Ethics application status
Approved
Date submitted
8/06/2011
Date registered
8/06/2011
Date last updated
5/07/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Patient outcomes after open and minimally invasive surgery for prostate cancer
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Scientific title
Patient outcomes after open and minimally invasive surgery for prostate cancer
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Secondary ID [1]
259916
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Localised Prostate Cancer
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Condition category
Condition code
Cancer
265680
265680
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0
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Prostate
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Surgery
268181
268181
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0
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Surgical techniques
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Patient outcomes after open radical prostatectomy for localised prostate cancer using repeated measures for 24 months after surgery.
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Intervention code [1]
266733
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Not applicable
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Comparator / control treatment
Patient outcomes after robot assisted radical prostatectomy and laparoscopic prostatectmy for localised prostate cancer using repeated measures for 24 months after surgery.
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Control group
Active
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Outcomes
Primary outcome [1]
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Functional and Psychosocial Status using the following:
SF36v2, HADS, AQoL-8D, Prostate Cancer Quality of Life Scale.
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Assessment method [1]
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Timepoint [1]
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baseline, 7 days, 4 weeks, 3 months, 6 months, 12 months, 18 months, 24 months
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Primary outcome [2]
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Sexual function using the following:
SHIM, EPIC (sexual), Prostate Cancer Quality of Life Scale (sexual intimacy)
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Assessment method [2]
266456
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Timepoint [2]
266456
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baseline, 7 days, 4 weeks, 3 months, 6 months, 12 months, 18 months, 24 months
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Primary outcome [3]
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Urinary function using the following:
SHIM, EPIC (urinary), Prostate Cancer Quality of Life Scale (urinary control)
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Assessment method [3]
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Timepoint [3]
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baseline, 7 days, 4 weeks, 3 months, 6 months, 12 months, 18 months, 24 months
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Secondary outcome [1]
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Pain Intensity and quality using the American Pain Society Patient Outcome Questionnaire (APSPOQ), McGill Pain Questionnaire short form (MPQSF)
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Assessment method [1]
273809
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Timepoint [1]
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postoperative, 7 days, 4 weeks
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Secondary outcome [2]
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wound healing by assessing wound apposition, infection and time to removal of sutures.
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Assessment method [2]
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Timepoint [2]
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postoperative, 7 days, 4 weeks
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Secondary outcome [3]
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Length of hospital stay measured from Day 1 (where Day 0 is day of surgery) to day of discharge from hospital inclusive.
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Assessment method [3]
273811
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Timepoint [3]
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At time of discharge.
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Secondary outcome [4]
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decisional regret measured using the Decisional Regret Scale and the Prostate Cancer Quality of Life Scale (regret)
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Assessment method [4]
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Timepoint [4]
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4 weeks, 3 months, 6 months, 12 months, 18 months, 24 months
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Eligibility
Key inclusion criteria
Patients undergoing Radical Retropubic Prostatectomy, Robot Assisted Radical Prostatectomy and Laparascopic Radical Prostatectomy for localised prostate cancer, admitted for elective surgery, over the age of 18 years and under the care of urology surgeons listed as Investigators.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients who are unable to provide informed consent to participate.
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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
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
12/01/2009
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Actual
12/01/2009
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Date of last participant enrolment
Anticipated
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Actual
14/02/2013
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Date of last data collection
Anticipated
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Actual
25/03/2015
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Sample size
Target
450
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Accrual to date
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Final
1055
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment postcode(s) [1]
4069
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3144
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Recruitment postcode(s) [2]
4070
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3121
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Funding & Sponsors
Funding source category [1]
264801
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Charities/Societies/Foundations
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Name [1]
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Prostate Cancer Foundation Australia
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Address [1]
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Level 3
39-41 Chandos St
St Leonards NSW 2065
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Country [1]
264801
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Australia
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Primary sponsor type
Individual
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Name
Mari Botti
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Address
School of Nursing and Midwifery
Deakin University
221 Burwood Highway
Burwood Victoria 3125
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Country
Australia
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Secondary sponsor category [1]
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Other Collaborative groups
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Name [1]
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Patient Outcomes after Prostate Surgery Investigators
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Address [1]
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Epworth HealthCare
89 Bridge Road
Richmond Victoria 3121
Cabrini Health
183 Wattletree Road
Malvern Victoria 3144
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Country [1]
266284
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
269208
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Deakin University Human Research and Ethics Committee
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Ethics committee address [1]
269208
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Deakin University 221 Burwood Highway Burwood Victoria 3125
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Ethics committee country [1]
269208
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Australia
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Date submitted for ethics approval [1]
269208
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Approval date [1]
269208
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04/05/2009
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Ethics approval number [1]
269208
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EC34-2009
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Ethics committee name [2]
269209
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Epworth Healthcare Human Research Ethics Committee
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Ethics committee address [2]
269209
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Epworth HealthCare 89 Bridge Road Richmond Victoria 3121
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Ethics committee country [2]
269209
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Australia
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Date submitted for ethics approval [2]
269209
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Approval date [2]
269209
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05/11/2008
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Ethics approval number [2]
269209
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42808
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Ethics committee name [3]
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Cabrini Human Research Ethics Committee
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Ethics committee address [3]
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Cabrini Health 183 Wattletree Road Malvern Victoria 3144
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Ethics committee country [3]
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Australia
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Date submitted for ethics approval [3]
269210
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Approval date [3]
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07/08/2006
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Ethics approval number [3]
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02-10-07-06
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Summary
Brief summary
The aim of this project is to evaluate and compare patients' physiological, functional and psychosocial recovery after three forms of radical prostatectomy surgery (open radical retropubic prostatectomy and two approaches to minimally invasive surgery: robotic-assisted radical prostatectomy and laparoscopic radical prostatectomy) for localised prostatic cancer. Recovery will be evaluated using repeated measures during three key transitions: acute (time in hospital), intermediate (7 days and 4 weeks after surgery) and long term (3 months, 6 months, 12, 18 and 24 months post surgery). The three cohorts of patients will be matched for age and prostate cancer-related criteria. Baseline preoperative assessment of patients will include: demographic characteristics, functional status including urinary and sexual function, and psychosocial status. Recovery variables will include repeated measures of: pain intensity and quality, wound healing, functional and psychosocial status.
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Trial website
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Trial related presentations / publications
Study protocol http://hdl.handle.net/10536/DRO/DU:30108464
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Public notes
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Contacts
Principal investigator
Name
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Prof Mari Botti
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Address
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Deakin University Geelong,
Faculty of Health
Victoria 3220
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Country
32437
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Australia
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Phone
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+61 3 94266565
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Fax
32437
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Email
32437
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[email protected]
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Contact person for public queries
Name
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Professor Mari Botti
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Address
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Deakin University
Faculty of Health
221 Burwood Highway
Burwood Victoria 3125
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Country
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Australia
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Phone
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61 3 94266565
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Fax
15684
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Email
15684
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[email protected]
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Contact person for scientific queries
Name
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Professor Mari Botti
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Address
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Deakin University
Faculty of Health
221 Burwood Highway
Burwood Victoria 3125
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Country
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Australia
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Phone
6612
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61 3 94266565
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Fax
6612
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Email
6612
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[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
No additional documents have been identified.
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