Het VISTA onderzoek:Het VTE-predictiemodel als leidraad voor de duur van antistollingstherapie binnen de huidige richtlijnen voor patiënten met een veneuze-tromboembolie.
- Conditions
- (Recurrent) Venous thromboembolismDeep vein thrombosisPulmonary Embolism(recidief) veneuze trombo-emboliediep veneuze tromboselongembolieVKA treatment durationrecurrent VTE prediction model
- Registration Number
- NL-OMON25558
- Lead Sponsor
- trecht University/ Utrecht University Medical Center
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 1500
Inclusion Criteria
1. First unprovoked VTE;
2. Legal age (>18 years).
Exclusion Criteria
1. Treatment indication VKA of at least 1 year
ie. recurrent VTE; atrial fibrillation; prosthetic valve;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Recurrent VTE during 24 months of follow-up after the initial 6 months of VKA treatment. VTE is defined as proximal DVT and/or fatal or non-fatal PE as confirmed by compression US for DVT and by (spiral CT) angiography and/or ventilation-perfusion lung scanning for PE.
- Secondary Outcome Measures
Name Time Method 1. The occurrence of major bleedings;<br /><br>2. Quality of life (based on QoL questionnaires at T=12 and T=24 months);<br /><br>3. Cost-effectiveness (at T=24 months using a Markov decision model).