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Clinical Trials in Taiwan / NCT05818072
Recruiting Not applicable

The Prevalence, Risk Factors and Optimal Biopsy Protocol of BE

NCT05818072 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2023-03-13
Last updated
2023-05-11

Condition(s) studied

Barrett's EsophagusIntestinal Metaplasia

Investigational drug(s) / intervention(s)

One biopsyThree biopsySeattle protocolEndoscopy

One biopsy: To do one biopsy at the proximal part of the longest columnar-lined esophagus.

Three biopsy: To do three biopsy at the proximal, middle and distal part of the longest columnar-lined esophagus.

Seattle protocol: To do 4-quadrant biopsy every 1-2 cm at the esophagogastric junction. Seattle protocol has been considered as the gold standard biopsy protocol for patients with suspected Barrett's Esophagus.

Endoscopy: The participants will receive meticulous endoscopic examination with narrow-band imaging.

Study summary

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.

Eligibility

Sex
ALL
Min age
20 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults with columnar-lined esophagus Exclusion Criteria: * A prior history of endoscopic treatment for Barrett's Esophagus * A prior history of upper gastrointestinal malignancy * A prior history of total or subtotal gastrectomy * Esophageal varices noted during the procedure * Uncontrolled coagulopathy * Taking antiplatelet drug or anticoagulant

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
E-DA Hospital Kaohsiung City Taiwan Recruiting

More E-DA Hospital trials in Taiwan

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05818072 on ClinicalTrials.gov ↗ ← All trials in Taiwan