Individually tailored elastic compression therapy after deep venous thrombosis in relation to the incidence of post thrombotic syndrome, a randomized multicenter trial
Recruiting
- Conditions
- post phlebetic syndrome1006447710014523
- Registration Number
- NL-OMON38265
- Lead Sponsor
- interne geneeskunde laboratorium hematologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 864
Inclusion Criteria
All adult, consenting, consecutive outpatients with acute objectively documented proximal DVT of the leg
•All patients should be treated with a minimum of 5 days of Low Molecular Weight Heparins (LMWH) followed by oral anticoagulants with a target international normalized ratio (INR) of 2-3
Exclusion Criteria
Previous DVT in the affected leg
•Recurrent DVT in the 6 months following inclusion
•Pre-existent venous insufficiency (skin signs C3-C6 on CEAP score or requiring ECS therapy)
•Contraindication for elastic compression therapy (e.g. arterial insufficiency)
•Active thrombolysis
•Life expectancy < 6 months
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method