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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT01562158
Registration number
NCT01562158
Ethics application status
Date submitted
22/03/2012
Date registered
23/03/2012
Date last updated
11/01/2017
Titles & IDs
Public title
Efficacy and Safety of Activated Recombinant Human Factor VII in Treatment of Bleeding in Patients Following Allogeneic Stem Cell Transplantation
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Scientific title
A Multi-centre, Randomised, Double-blind, Parallel Groups, Placebocontrolled Trial on Efficacy and Safety of Activated Recombinant Factor VII (rFVIIa/NovoSeven®) in Treatment of Bleeding in Patients Following Stem Cell Transplantation (SCT)
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Secondary ID [1]
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F7BMT-1360
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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:
Acquired Bleeding Disorder
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Bleeding During/Following Surgery
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Condition category
Condition code
Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Blood
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Clotting disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Surgery - standard therapy
Treatment: Drugs - activated recombinant human factor VII
Treatment: Drugs - activated recombinant human factor VII
Treatment: Drugs - activated recombinant human factor VII
Treatment: Drugs - placebo
Placebo comparator: Placebo -
Experimental: Low dose -
Experimental: Medium dose -
Experimental: High dose -
Treatment: Surgery: standard therapy
Standard treatment of bleeding
Treatment: Drugs: activated recombinant human factor VII
Two days repeated treatment regimen - low dose administered i.v. (into the vein)
Treatment: Drugs: activated recombinant human factor VII
Two days repeated treatment regimen - medium dose administered i.v. (into the vein)
Treatment: Drugs: activated recombinant human factor VII
Two days repeated treatment regimen - high dose administered i.v. (into the vein)
Treatment: Drugs: placebo
Placebo
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Intervention code [1]
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Treatment: Surgery
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Intervention code [2]
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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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Effect on bleeding, defined as change in bleeding score
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [1]
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Transfusion requirements
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [2]
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Bleeding evaluation
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Assessment method [2]
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Timepoint [2]
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Secondary outcome [3]
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Adverse events
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Assessment method [3]
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Timepoint [3]
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Eligibility
Key inclusion criteria
* Patients who have undergone allogeneic or autologous stem cell transplantation
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Minimum age
12
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
* Known or suspected allergy to trial product
* Participation in other trials with unapproved drugs or trials with equal or similar objective
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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 analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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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
1/04/2001
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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
1/10/2003
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Sample size
Target
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Accrual to date
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Final
100
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Novo Nordisk Investigational Site - Herston
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Recruitment hospital [2]
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Novo Nordisk Investigational Site - Parkville
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Recruitment hospital [3]
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Novo Nordisk Investigational Site - Westmead
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Recruitment postcode(s) [1]
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4029 - Herston
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Recruitment postcode(s) [2]
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3050 - Parkville
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Recruitment postcode(s) [3]
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2145 - Westmead
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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North Carolina
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Austria
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Vienna
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Denmark
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København
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Finland
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Helsinki
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France
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Besancon
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France
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Lille
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France
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Tours
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Germany
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Dresden
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Germany
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Hamburg
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Germany
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Hannover
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Germany
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Idar-Oberstein
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Germany
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Köln
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Germany
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München
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Germany
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Germany
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Tübingen
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Germany
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Wiesbaden
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Israel
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Haifa
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Israel
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Jerusalem
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Italy
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Firenze
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Italy
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Genova
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Italy
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Pesaro
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Italy
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Rome
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Italy
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Udine
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Gdansk
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Poznan
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Warszawa
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Wroclaw
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Singapore
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Singapore
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Spain
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Barcelona
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Spain
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Santander
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Spain
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Valencia
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Sweden
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Göteborg
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Sweden
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Stockholm
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Sweden
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Uppsala
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Switzerland
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Basel
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Switzerland
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Zürich
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Thailand
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Bangkok
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United Kingdom
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London
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United Kingdom
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Manchester
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Novo Nordisk A/S
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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
This trial is conducted in Asia, Europe and Oceania. The aim of this trial is to evaluate the efficacy of placebo and activated recombinant human factor VII in patients having undergone allogeneic or autologous stem cell transplantation.
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Trial website
https://clinicaltrials.gov/study/NCT01562158
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Trial related presentations / publications
Pihusch M, Bacigalupo A, Szer J, von Depka Prondzinski M, Gaspar-Blaudschun B, Hyveled L, Brenner B; F7BMT-1360 Trial Investigators. Recombinant activated factor VII in treatment of bleeding complications following hematopoietic stem cell transplantation. J Thromb Haemost. 2005 Sep;3(9):1935-44. doi: 10.1111/j.1538-7836.2005.01523.x.
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Public notes
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Contacts
Principal investigator
Name
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Global Clinical Registry (GCR, 1452)
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Address
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Novo Nordisk A/S
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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
Type
Citations or Other Details
Journal
Pihusch M, Bacigalupo A, Szer J, von Depka Prondzi...
[
More Details
]
Results not provided in
https://clinicaltrials.gov/study/NCT01562158
Download to PDF