Efficacy Test of Real-Time Upper Gastrointestinal Monitoring System

Status Completed

Clinical Trial Summary

A monitoring system was developed for detecting upper gastrointestinal (UGI) rebleeding. This system consists of (1) a tiny endoscopy, (2) a wearable device, and (3) a software. The endoscopy is inserted to UGI tract via nasal cavity and then stayed there for 3 days. The wearable device is set to regularly receive the pictures from the endoscopy and sent to the software, which is able to automatically analyze whether the rebleeding occurs. This study aims to test the feasibility and efficacy of the monitoring system.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03680950
Study type	Interventional
Source	National Cheng-Kung University Hospital
Contact
Status	Completed
Phase	N/A
Start date	October 12, 2018
Completion date	April 30, 2020

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