Shared Decision-making Process for Unprovoked vEnous THromboEmbolism Management. (ETHER )
Recruiting
N/A
Interventional Study
Venous Thromboembolism
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 2,400 (estimated)
- Sponsor
- University Hospital, Brest · Other
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About This Trial
Venous thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE) is a frequent disease and the third most common cause of cardiovascular death in the world after myocardial infarction and stroke. Anticoagulant therapy drastically reduces the risk of early VTE recurrence and death, but it exposes patients to a substantial risk of bleeding. Hence, determining the optimal…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient \> or = 18 years,
* Patient with a first episode of symptomatic unprovoked pulmonary embolism (PE) and/or proximal deep vein thrombosis (DVT) treated for 3 to 6 uninterrupted months with full dose anticoagulant therapy,
* Signed informed consent.
Exclusion Criteria:
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Contacts