Comparitive study of the stability of oral anticoagulant therapy using phenprocoumon or warfarin.
Completed
- Registration Number
- NL-OMON23351
- Lead Sponsor
- eiden University Medical Center
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 500
Inclusion Criteria
1. No current use of anticoagulants;
2. Aged 18–85;
Exclusion Criteria
1. Pregnancy;
2. Chemotherapy;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time spent within therapeutic range, time to the first INR in range, percentage of INRs above range after initiation scheme, reaction of INR to interruption of coumarin or vitamin K administration.
- Secondary Outcome Measures
Name Time Method 1. Bleeding complications; <br /><br>2. Thrombotic complications.