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NCT05818072

The Prevalence, Risk Factors and Optimal Biopsy Protocol of BE

Recruiting now NA Last updated 11 May 2023
What this trial tests

NA trial testing One biopsy in Barrett's Esophagus in 165 participants. Currently enrolling.

Timeline
13 March 2023
Primary endpoint
31 December 2025
31 December 2026

Quick facts

Lead sponsorE-DA Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposediagnostic
Enrollment165
Start date13 March 2023
Primary completion31 December 2025
Estimated completion31 December 2026
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

E-DA Hospital

Who can join

20 and older, any sex, with Barrett's Esophagus or Intestinal Metaplasia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Detections of goblet cells and dysplasia are crucial for diagnosis and determining the surveillance program of Barrett's esophagus (BE). However, the optimal biopsy numbers and their yield rates of intestinal metaplasia (IM) and dysplasia are still uncertain, especially in Asia. The aim of this study was to determine the optimal biopsy protocol of BE.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Barrett's Esophagus

Currently open trials in the same condition.

Other E-DA Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05818072.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing