PRospective Evaluation of Peripartum Anticoagulation ManaGement for ThrOmboembolism (NCT05756244)
A Prospective Cohort Study Evaluating Peripartum Anticoagulation Management Among Pregnant Women With Venous Thromboembolism and Its Impact on Patient Outcomes
๐ฉบ Plain-English Summary (8th-Grade Level)
The PREP and GO study is an international multicentre prospective cohort evaluating anticoagulation management strategies around labor and delivery and the postpartum period.
Who can join: Review the eligibility criteria below.
Location: Duke University Hospital โ Durham, North Carolina
Age range: 18 Years to 60 Years
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (14 Sites)
- Duke University Hospital โ Durham, North Carolina
- Foothills Medical Centre โ Calgary, Alberta
- Royal Alexandra Hospital โ Edmonton, Alberta
- BC Women's Hospital and Health Centre โ Vancouver, British Columbia
- St. Boniface Hospital โ Winnipeg, Manitoba
- McMaster University Medical Centre โ Hamilton, Ontario
- The Ottawa Hospital - General Campus โ Ottawa, Ontario
- Montfort Hospital โ Ottawa, Ontario
- Mount Sinai Hospital โ Toronto, Ontario
- CHU Sainte-Justine โ Montreal, Quebec
- The Sir Mortimer B. Davis Jewish General Hospital โ Montreal, Quebec
- Aarhus University Hospital โ Aarhus,
- Le Centre Hospitalier Universitaire of Saint-Etienne โ Saint-Etienne,
- Hopitaux universitaires de Geneve โ Geneva,
๐ Contact the Study Coordinator
Phone: (403) 220-7103
Email: jbaxter@ucalgary.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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- Elevating Voices, Addressing Depression, Toxic Stress and Equity in Group Prenatal Care โ Kansas City, Missouri
- Well-Mama Community Doula Navigator Study โ Baton Rouge, Louisiana
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Explore by condition: All Pregnancy Related clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.