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NCT06938919

Electronic Respiratory Sound Monitoring System in Gastrointestinal Endoscopic Sedation

Completed NA Last updated 28 January 2026
What this trial tests

NA trial testing routine care without electronic respiratory sound monitoring system in Gastrointestinal Endoscope in 200 participants. Completed in 13 November 2025.

Timeline
29 May 2025
Primary endpoint
13 November 2025
13 November 2025

Quick facts

Lead sponsorNational Taiwan University Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment200
Start date29 May 2025
Primary completion13 November 2025
Estimated completion13 November 2025
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

National Taiwan University Hospital

Who can join

Adults 18 to 99, any sex, with Gastrointestinal Endoscope or Endoscopic Retrograde Cholangiopancreatogram (ERCP). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to evaluate the application of an electronic respiratory sound monitoring system during sedation for gastrointestinal endoscopy and to determine its effectiveness in improving sedation quality. Gastrointestinal endoscopy is a common medical procedure, but respiratory complications caused by sedation, such as hypoventilation and airway obstruction, are significant safety concerns. Traditional respiratory monitoring methods, such as end-tidal CO2 monitoring, are often unreliable due to difficulties in gas sampling during the procedure. In contrast, an electronic respiratory sound monitoring system can accurately capture tracheal breathing sounds and provide important parameters such as respiratory rate and airway obstruction ratio, helping clinicians avoid over-sedation. This study will conduct a randomized controlled trial with 120 participants, divided into a control group with conventional monitoring and an experimental group using the electronic respiratory sound monitoring system. The study will compare sedation dosage, airway complications, and recovery speed between the two groups, and further analyze the clinical value of the system's parameters. The findings of this study will contribute to improving the safety and precision of sedation during gastrointestinal endoscopy and provide evidence for future clinical guidelines.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other National Taiwan University Hospital trials

Trials by the same sponsor.

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