A Personalized Surveillance and Intervention Protocol for Patients With Familial Adenomatous Polyposis That Have Undergone (Procto)Colectomy (NCT04678011)

🧪 Interventions in This Study

• Personalized surveillance and intervention protocol (PROCEDURE)

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

📍 All Participating Trial Locations (2 Sites)

• MD Anderson — Houston, Texas
• Academic Medical Centre — Amsterdam, North Holland

📞 Contact the Study Coordinator

Phone: (919) 923-4430

Email: aglincoln@mdanderson.org

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.

More studies in Familial Adenomatous Polyposis

• Trial of ERapa to Prevent Progression in Familial Adenomatous Polyposis Patients Under Active Surveillance — Ann Arbor, Michigan
• A Personalized Surveillance and Intervention Protocol for Duodenal and Gastric Polyposis in Patients With Familial Adenomatous Polyposis — Houston, Texas
• Trial of Exercise Therapy in Familial Adenomatous Polyp (FAP) — Ann Arbor, Michigan
• Evaluate REC-4881 in Participants With Familial Adenomatous Polyposis (FAP) — Scottsdale, Arizona

Explore by condition: All Familial Adenomatous Polyposis clinical trials

💡 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.