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

Part of paid clinical trials in Houston, Texas.

Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Study ID
NCT04678011
Status
Recruiting
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Conditions

  • Familial Adenomatous Polyposis

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Personalized surveillance and intervention protocol — PROCEDURE
    This study uses one arm. Participants will undergo endoscopic surveillance with intervals between 6 months and 2 years, depending on severity of polyposis and performed endoscopic interventions.

Study Details

The purpose of this study is to determine the efficacy and safety of a personalised surveillance and intervention protocol for patients with familial adenomatous polyposis (FAP) that have undergone (procto)colectomy.

Key Dates

Start date
Nov 24, 2021
Status verified
Sep 2025
Primary completion
Nov 30, 2026
Completion
Nov 30, 2026

Study Design

Enrollment
1,000 participants (estimated)

Arms

  • Arm: Personalized surveillance and intervention protocol

Primary Outcome Measure

Advanced neoplasia [ Time Frame: Up to 5 years ]

Locations (1)

FacilityCityStateZIPSite coordinators
MD AndersonHoustonTexas77030
Annie Lincoln
[email protected]
+1 919 923 4430
Luigi Ricciardiello (PRINCIPAL_INVESTIGATOR)

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By research site
MD Anderson· Houston, TX

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