Barrett's Esophagus Clinical Trial
Official title:
APE-Study: Tumor-free Survival After Ablation of Barrett's Mucosa Plus Esomeprazole vs. Surveillance Without Ablation in Patients Cured From Barrett's Cancer Combined With Randomization of Esomeprazole vs Placebo for Symptomatic Reflux Control After Successful Ablation of Barrett's Mucosa
This is a prospective, randomized, controlled, double-blinded, multi-center trial in a
parallel-group design. Aim of the study is the evaluation of tumor-free survival after
ablation (by APC, argon plasma coagulation) of Barrett's mucosa plus esomeprazole versus
surveillance without ablation in patients cured from Barrett's cancer combined with
randomization of esomeprazole vs placebo for symptomatic reflux control after successful
ablation of Barrett's mucosa .
There are two hypotheses: (1) Consecutive thermal ablation of metaplastic, non-neoplastic
long segments of Barrett's esophagus (>2cm)plus esomeprazole after successful endoscopic
therapy of mucosal cancer by means of ER will decrease the incidence of secondary cancer
(local recurrence and metachronous cancer) by a minimum of 50% compared to acid suppression
alone without ablation within a 5-years follow-up (primary endpoint). (2) After successful
ablation of Barrett's esophagus patients need ongoing acid suppression therapy for medical
control of their underlying reflux disease (secondary aim of the study).
Duration of the study:
Patient recruitment period: 3 years. Follow-up period: 5 years. Total duration: 8 years. The
study is already in the recruitment period.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
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