Global Anticoagulant Registry in the FIELD- Venous Thromboembolic Events
Completed
Conditions studied: Venous Thromboembolism, Deep Vein Thrombosis, Pulmonary Embolism
In brief
The protocol is a large registry to describe acute, sub-acute and extended duration of anticoagulation management, clinical and economic duration of anticoagulation management, clinical and economic outcomes in patients with treated acute VTE (DVT and PE) in the real-world setting. Main objectives are to clarify the: * treatment related details for acute VTE (either conventional anticoagulation therapy, treatment with a direct oral anti-coagulant or other modalities of treatment) * Rate of early and late symptomatic VTE recurrence * Rate and nature of complications of VTE including post thrombotic syndrome and chronic thromboembolic pulmonary hypertension * Rate of bleeding complications * Rate of all-cause mortality at six months
Key facts
- Study ID
- NCT02155491
- Run by
- Thrombosis Research Institute
- People needed
- 10679
- Starts
- 2014-07-07
- Expected to finish
- 2020-09-30
- Last updated by the study team
- 2021-05-05
Who can join
Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Written informed consent
- Age 18 years and over
- Treated first time or recurrent DVT (lower or upper extremity), PE alone or overlapping DVT and PE confirmed by appropriate diagnostic methods (patients must be assessed for eligibility within 30 days of diagnosis)
- Patients included with recurrent VTE must have completed treatment for the previous VTE episode
You may not qualify if…
- Patients for whom long-term follow-up is not envisaged within the enrolling hospital or the associated primary care physician
- Patients participating in an interventional study that dictates treatments, visit frequency, or diagnostic procedures
- Patients with only superficial vein thrombosis (SVT)
Where it is running
- Dr Terence Hart — Muscle Shoals, Alabama, United States
Full record on ClinicalTrials.gov
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