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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00074906
Registration number
NCT00074906
Ethics application status
Date submitted
23/12/2003
Date registered
25/12/2003
Date last updated
7/05/2012
Titles & IDs
Public title
Venticute in Patients With Pneumonia or Aspiration of Gastric Contents and Intubation/Ventilation/Oxygenation Impairment (BY2001/M1-007)
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Scientific title
Venticute in Patients With Pneumonia or Aspiration of Gastric Contents Leading to Intubation, Ventilation, and Severe Oxygenation Impairment: A Randomized, Multinational, Multicenter, Parallel Group, Double Blind, Control Group Study
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Secondary ID [1]
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BY2001/M1-007
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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:
Pneumonia
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Condition category
Condition code
Respiratory
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Other respiratory disorders / diseases
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Infection
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Other infectious diseases
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Infection
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Studies of infection and infectious agents
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Venticute
Treatment: Drugs: Venticute
Patients With Pneumonia or Aspiration of Gastric Contents and Intubation/Ventilation/Oxygenation Impairment
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Survival on day 28
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Assessment method [1]
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Timepoint [1]
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28 days
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Secondary outcome [1]
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How long the lung and the patient (overall) are recovering
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Assessment method [1]
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Timepoint [1]
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28 days
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Eligibility
Key inclusion criteria
Main inclusion criteria:
* Patient has been intubated due to one of the following primary pulmonary insults: aspiration of gastric contents or pneumonia
Main exclusion criteria:
* Principal source of infection or sepsis is outside the lung
* Severe pre-existing lung disease
* Cancer metastatic to the lung or any end stage malignancy
* History of lung, liver, pancreas, small bowel, or bone marrow/stem cell transplantation
* Patient is morbidly obese
* Patient has a diagnosis of acute necrotizing pancreatitis
Additional criteria may apply and examination by an investigator is required to determine eligibility.
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Minimum age
12
Years
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Maximum age
85
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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
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/11/2003
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/06/2008
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Sample size
Target
1200
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Altana Pharma/Nycomed - Adelaide SA
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Recruitment hospital [2]
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Altana Pharma/Nycomed - Bedford Park, Adelaide S
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Recruitment hospital [3]
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Altana Pharma/Nycomed - Clayton, VIC
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Altana Pharma/Nycomed - Fremantle, WA
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Altana Pharma/Nycomed - Heidelberg, Victoria
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Altana Pharma/Nycomed - Kingswood, Sydney, NS
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Altana Pharma/Nycomed - Melbourne VIC
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Altana Pharma/Nycomed - Perth, Western Australi
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Altana Pharma/Nycomed - Southport Gold Coast QL
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Altana Pharma/Nycomed - Victoria
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Altana Pharma/Nycomed - Woolloongabba, Queens
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5000 - Adelaide SA
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5042 - Bedford Park, Adelaide S
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3158 - Clayton, VIC
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6959 - Fremantle, WA
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3084 - Heidelberg, Victoria
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2750 - Kingswood, Sydney, NS
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3004 - Melbourne VIC
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6000 - Perth, Western Australi
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Recruitment postcode(s) [9]
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4215 - Southport Gold Coast QL
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3050 - Victoria
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Recruitment postcode(s) [11]
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3128 - Victoria
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Recruitment postcode(s) [12]
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4102 - Woolloongabba, Queens
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Recruitment outside Australia
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Austria
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Linz
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Austria
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Brussels
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Copenhagen NV
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Oulu
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Kings Lynn, Norfolk
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West Lothian
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Takeda
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Study to demonstrate that administration of Venticute increases survival of patients with pneumonia or aspiration of gastric contents leading to intubation, mechanical ventilation, and severe oxygenation impairment.
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Trial website
https://clinicaltrials.gov/study/NCT00074906
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Trial related presentations / publications
Spragg RG, Taut FJ, Lewis JF, Schenk P, Ruppert C, Dean N, Krell K, Karabinis A, Gunther A. Recombinant surfactant protein C-based surfactant for patients with severe direct lung injury. Am J Respir Crit Care Med. 2011 Apr 15;183(8):1055-61. doi: 10.1164/rccm.201009-1424OC. Epub 2010 Dec 10.
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Public notes
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Contacts
Principal investigator
Name
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Roger G. Spragg, MD
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Address
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University of California and La Jolla Veterans Affairs Medical Center, San Diego, CA, USA
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Contact person for scientific queries
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
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00074906
Download to PDF