Artificial Intelligence-Guided Detection of Blood Vessels to Enhance Safety in Third-Space Endoscopic Procedures

NCT07399652 · tracked via the Priya Life Science India tracker

Sponsor

Asian Institute of Gastroenterology, India

Phase

Not applicable

Started

2026-02-10

Last updated

2026-04-15

Condition(s) studied

Achalasia CardiaTumor

Investigational drug(s) / intervention(s)

AI generated segmentation mask for sub-mucosal blood vessels

AI generated segmentation mask for sub-mucosal blood vessels: Real time AI generated segmentation mask or delineation contours for sub-mucosal blood vessels visible on the endoscopy monitor.

Study summary

This prospective study aims to evaluate the performance of a novel Artificial Intelligence (AI) clinical decision support tool during third space endoscopic procedures, such as Endoscopic Submucosal Dissection (ESD) and Peroral Endoscopic Myotomy (POEM).

While these procedures are effective for treating gastrointestinal neoplasms and motility disorders, they carry risks of intraprocedural bleeding and perforation if submucosal blood vessels are not correctly identified and coagulated. Building on previous retrospective validation, this study will assess whether a real-time artificial intelligence model can assist endoscopists in detecting and delineating blood vessels more accurately and faster during live human procedures.

Eligibility

Sex

ALL

Min age

—

Max age

—

Healthy volunteers

Inclusion Criteria: * Patients diagnosed with Achalasia Cardia or neoplasms. Exclusion Criteria: * Patients with conditions deemed unsuitable for third space endoscopy procedures (e.g.: Candidiasis)

Primary outcome measure(s)

Vessel Detection Rate (VDR) — 3 months
the proportion of vessels identified by the endoscopist

Trial sites (1)

Facility	City	Region	Status
Asian Institute of Gastroenterology	Hyderabad	Telangana	Recruiting

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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 NCT07399652 on ClinicalTrials.gov ↗ ← All trials in India