Registry of Patients Prescribed Anticoagulation for VTE
This study is a registry, which means it collects information from routine medical care, for patients who are prescribed blood thinners (anticoagulation) after being diagnosed with a blood clot (venous thromboembolism or VTE). This includes deep vein thrombosis (DVT) or pulmonary embolism (PE). You can join if you are 18 or older and start anticoagulation treatment within 14 days of your VTE diagnosis at the Mayo Clinic's Thrombophilia Clinic in Rochester, Minnesota. You cannot join if you are already taking blood thinners for other reasons or are in another blood thinner clinical trial. The study aims to track how often patients experience another blood clot or major bleeding over 10 years.
- Study design
- This is an observational study, meaning it collects information from your regular medical care without assigning specific treatments. It aims to include about 10,000 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will track outcomes like recurrent blood clots and major bleeding for up to 10 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Registry of Patients Prescribed Anticoagulation
At a glance
Conditions
NCT03504007
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Mayo Clinic
Rochester, Minnesotastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Damon Houghton, MD, MS · PRINCIPAL_INVESTIGATOR · Mayo Clinic
Who to contact
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Exclusion
What this trial measures
- Incidence of symptomatic, recurrent VTE. Incidence of major bleeding10 years
Recurrent VTE clearly new compared to previous VTE. Major bleeding by ISTH definition