🏛️ Verified NIH Record • Updated 2025-07-03

Primary Thromboprophylaxis in Patients With Malignancy and Central Venous Catheters (NCT05029063)

Primary Thromboprophylaxis in Patients With Malignancy and Central Venous Catheters: a Randomized Controlled Trial

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Ottawa Hospital Research Institute

🩺 Plain-English Summary (8th-Grade Level)

The purpose of the full trial is to determine the efficacy and safety of prophylactic dose rivaroxaban to prevent VTE among cancer patients with CVC.

Who can join: Review the eligibility criteria below.

Location: Nova Scotia Health — Halifax, Nova Scotia

Age range: 18 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (11 Sites)

  • Nova Scotia Health — Halifax, Nova Scotia
  • William Osler Health System — Brampton, Ontario
  • HHS - Juravinski Hospital — Hamilton, Ontario
  • Ottawa Hospital Research Institute- The Ottawa Hospital — Ottawa, Ontario
  • Sault Area Hospital — Sault Ste. Marie, Ontario
  • Niagara Health — St. Catharines, Ontario
  • Windsor Regional Hospital — Windsor, Ontario
  • CISSS Montérégie-Centre HOPITAL CHARLES LEMOYNE — Greenfield Park, Quebec
  • Centre Intégré de santé et de services sociaux de Chaudière-Appalaches — Lévis, Quebec
  • Jewish General Hospital — Montreal, Quebec
  • McGill University Health Center — Montreal, Quebec

📞 Contact the Study Coordinator

Phone: (613) 737-8899

Email: byazji@ohri.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 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 § 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.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗