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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00790920
Registration number
NCT00790920
Ethics application status
Date submitted
13/11/2008
Date registered
14/11/2008
Date last updated
18/09/2015
Titles & IDs
Public title
Efficacy and Safety Study of Desmoteplase to Treat Acute Ischemic Stroke
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Scientific title
A Randomised, Double-blind, Parallel-group Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of Desmoteplase in Subjects With Acute Ischemic Stroke
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Secondary ID [1]
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2008-000622-40
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Secondary ID [2]
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12402A
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Universal Trial Number (UTN)
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Trial acronym
DIAS-3
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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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Condition category
Condition code
Stroke
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Haemorrhagic
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Stroke
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Ischaemic
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Desmoteplase
Treatment: Drugs - Placebo
Experimental: Desmoteplase -
Placebo comparator: Placebo -
Treatment: Drugs: Desmoteplase
90 µg/kg bodyweight, IV, single bolus over 1 - 2 minutes on 1st day
Treatment: Drugs: Placebo
IV, single bolus over 1 - 2 minutes on 1st day
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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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Modified Rankin Scale Score
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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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National Institutes of Health Stroke Scale (NIHSS) Score
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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
* Diagnosis of acute ischemic stroke
* Informed consent
* Age between 18 and 85 years
* Treatment can be initiated within 3-9 hours after the onset of stroke symptoms
* NIHSS Score of 4-24
* Vessel occlusion or high-grade stenosis on MRI or CTA in proximal cerebral arteries
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Minimum age
18
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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
* Pre-stroke mRS >1
* Previous exposure to desmoteplase
* Extensive early infarction on MRI or CT in any affected area
* Imaging evidence of ICH or SAH; AV malformation; cerebral aneurysm; or cerebral neoplasm
* Internal carotid artery occlusion on the side of the stroke lesion
* Treatment with heparin in the past 48 hours and a prolonged partial thromboplastin time
* Treatment with oral anticoagulants and a prolonged prothrombin time
* Treatment with glycoprotein IIb - IIIa inhibitors within the past 72 hours. Use of single agent oral platelet inhibitors is permitted
* Treatment with a thrombolytic agent within the past 72 hours
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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 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
1/12/2008
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
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Actual
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Sample size
Target
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Accrual to date
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Final
492
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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AU006 - Clayton
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AU004 - Gosford
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AU001 - Melbourne
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AU002 - Melbourne
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AU003 - New Castle
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AU009 - Perth
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3168 - Clayton
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Recruitment postcode(s) [2]
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2250 - Gosford
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- Melbourne
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- New Castle
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6000 - Perth
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Recruitment outside Australia
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Austria
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Graz
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Austria
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Innsbruck
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
H. Lundbeck A/S
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of the study is to determine whether desmoteplase is effective and safe in the treatment of patients with acute ischaemic stroke when given within 3-9 hours from onset of stroke symptoms.
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Trial website
https://clinicaltrials.gov/study/NCT00790920
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Trial related presentations / publications
Albers GW, von Kummer R, Truelsen T, Jensen JK, Ravn GM, Gronning BA, Chabriat H, Chang KC, Davalos AE, Ford GA, Grotta J, Kaste M, Schwamm LH, Shuaib A; DIAS-3 Investigators. Safety and efficacy of desmoteplase given 3-9 h after ischaemic stroke in patients with occlusion or high-grade stenosis in major cerebral arteries (DIAS-3): a double-blind, randomised, placebo-controlled phase 3 trial. Lancet Neurol. 2015 Jun;14(6):575-84. doi: 10.1016/S1474-4422(15)00047-2. Epub 2015 Apr 30.
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Public notes
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Contacts
Principal investigator
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Email contact via H. Lundbeck A/S
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[email protected]
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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/NCT00790920
Download to PDF