A blind randomized trial to compare the efficacy of intermittent pneumatic compression (IPC) with and without early anticoagulant treatment for prevention of venous thromboembolism (VTE) in patients with acute primary intracerebral hemorrhage (ICH) including comparison of the American and European guideline recommendations
Phase 1
- Conditions
- Spontaani aivoverenvuotoMedDRA version: 9.1Level: LLTClassification code 10022754Term: Intracerebral hemorrhage
- Registration Number
- EUCTR2007-006206-24-FI
- Lead Sponsor
- Hillbom Matti OYS/neurologian klinikka
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method