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Outcomes for patients undergoing endoscopic therapy for Barrett’s related neoplasia: over 10-year experience from the Dutch Barrett Expert Centers

Recruiting
Conditions
Barrett's esophagus
Barrett's related neoplasia
Registration Number
NL-OMON29089
Lead Sponsor
ead site:Academic Medical Center Amsterdam (AMC)Collaborating centers:•Sint Antonius Hospital Nieuwegein•Catharina Hospital, Eindhoven•University Medical Center, Utrecht•Isala Clinics, Zwolle•Erasmus Medical Center, Rotterdam•Haga Hospital, Den Haag•University Medical Center, Groningen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
2000
Inclusion Criteria

1)Males or females, all ages

2)Presence of Barrett’s esophagus, with presence of intestinal metaplasia in histologic assessment.

Exclusion Criteria

1)Objection against participation in this study, through an opt-out card or e-mail

2)Referral for surgery after the work-up endoscopy for advanced EAC

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary objective is to determine the proportion of patients with successful eradication of BE after endoscopic therapy. The primary endpoint will be the proportion of patients with a successful complete eradication of Barrett’s neoplasia (CE-Neo) after the treatment phase.
Secondary Outcome Measures
NameTimeMethod
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