A Personalized Surveillance and Intervention Protocol for Duodenal and Gastric Polyposis in Patients With Familial Adenomatous Polyposis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

About this trial

The purpose of this study is to determine the efficacy and safety of a personalized surveillance and intervention protocol for duodenal and gastric polyposis in patients with familial adenomatous polyposis (FAP)

Eligibility criteria

Qualifiers

Diagnosis of FAP, at least one of following: genetic diagnosis (proven APC germline mutation) and/or clinical diagnosis (>100 colorectal adenomas in combination with a positive family history of FAP)

Age 18 years or older

Disqualifiers

Endoscopic removal of all polyps with an indication for removal not possible/feasible

Gastric or duodenal cancer at baseline endoscopy

Need for surgery

Trial design

Treatments tested in this trial

  • Personalized surveillance and intervention protocol

Treatment groups

1,000 Participants
are divided into 1 treatment group

Sponsors and collaborators

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Lead sponsor

Leiden University Medical Center

Collaborator

The Netherlands Cancer Institute

Collaborator

St Mark's Hospital Foundation

Collaborator

Hospital Clinic of Barcelona

Collaborator

Maria Sklodowska-Curie National Research Institute of Oncology

Collaborator

Hospital General Universitario de Alicante

Collaborator

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Collaborator

Radboud University Medical Center

Collaborator

University Hospital, Bonn

Collaborator

Hvidovre University Hospital

Collaborator

M.D. Anderson Cancer Center

Collaborator