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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00300196
Registration number
NCT00300196
Ethics application status
Date submitted
6/03/2006
Date registered
8/03/2006
Date last updated
12/01/2010
Titles & IDs
Public title
ASP-II: Ancrod Stroke Program: Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke
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Scientific title
ASP II (Ancrod Stroke Program) Study of Acute Viprinex™ for Emergency Stroke: A Randomized, Double-Blind, Placebo-Controlled Study of Ancrod (Viprinex™) in Subjects Beginning Treatment Within 6 Hours of the Onset of Acute Ischemic Stroke
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Secondary ID [1]
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NTI-ASP-0503
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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:
Stroke
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Cerebral Ischemia
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Brain Infarction
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Condition category
Condition code
Stroke
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Haemorrhagic
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Stroke
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Ischaemic
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Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Neurological
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Other neurological disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Other - Ancrod (Viprinex)
Treatment: Drugs - Placebo
Experimental: Intravenous ancrod - Intravenous ancrod infused at a rate of 0.167 IU/kg/hr (0.6 mL/kg/hr) for 2 or 3 hours depending on the pretreatment fibrinogen level.
Placebo comparator: Intravenous Placebo - Intravenous placebo at a rate of 0.6 mL/kg/hr for 2 or 3 hours depending on the pretreatment fibrinogen level.
Treatment: Other: Ancrod (Viprinex)
0.167 IU/kg/hr IV for 2-3 hours
Treatment: Drugs: Placebo
0.6 mL/kg/hr
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Intervention code [1]
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Treatment: Other
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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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Modified Rankin Score - responder analysis
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Assessment method [1]
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Timepoint [1]
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90 days
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Secondary outcome [1]
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Barthel Index, NIHSS
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Assessment method [1]
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Timepoint [1]
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90 days
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Eligibility
Key inclusion criteria
* Acute, ischemic stroke with first symptoms within 6 hours of beginning treatment
* Baseline NIHSS > 5
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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
* No intracranial, extravascular blood on CT
* Hypertension (systolic > 185; diastolic > 105)
* Baseline fibrinogen level < 100 mg/dL
* Thrombocytopenia (< 100,000 / mm3)
* Recent (< 3 days) or anticipated (< 5 days) use of a thrombolytic agent
* Recent (< 14 days) or anticipated surgery
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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 assessing the outcomes
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
Stopped early
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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
1/03/2006
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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
1/12/2008
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Sample size
Target
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Accrual to date
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Final
311
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
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Recruitment hospital [1]
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St Vincent's Hospital - Darlinghurst
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Gold Coast Hospital - Southport
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Moash Medical Center Dept of Neurology - Clayton
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Royal Melbourne Hospital - Parkville
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Alfred Hospital Research - Melbourne - Prahan, Melbourne
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Concord Hospital Neuroscience Department - New South Wales
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Recruitment postcode(s) [1]
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2010 - Darlinghurst
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- Southport
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3168 - Clayton
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3050 - Parkville
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Recruitment postcode(s) [5]
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3184 - Prahan, Melbourne
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Recruitment postcode(s) [6]
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- New South Wales
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Recruitment outside Australia
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United States of America
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California
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Connecticut
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Austria
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Graz
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Neurobiological Technologies
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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
The primary purpose of this study is to determine whether a brief intravenous infusion of ancrod started within 6 hours of stroke onset improves functional outcome at 3 months.
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Trial website
https://clinicaltrials.gov/study/NCT00300196
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Warren Wasiewski, M.D.
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Address
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Neurobiological Technologies
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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/NCT00300196
Download to PDF