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Capnographic Monitoring in Gastrointestinal Endoscopy for Elderly Patients

NCT05030870 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1800

Last updated 2024-03-19

No results posted yet for this study

Summary

Hypoxia is the most common adverse event in gastrointestinal endoscopes sedated with propofol and sufentanil, especially in elderly people. The aim of this randomized study was to determine whether intervention based on additional capnographic monitoring reduces the incidence of hypoxia in gastrointestinal endoscopes procedures for elderly patients.

Conditions

Interventions

DEVICE

Capnography monitoring

Standard monitoring and capnographic monitoring.

DEVICE

Standard monitoring

Standard monitoring but no capnographic monitoring

Sponsors & Collaborators

  • Henan Provincial People's Hospital

    collaborator OTHER

  • Qilu Hospital of Shandong University

    collaborator OTHER

  • RenJi Hospital

    lead OTHER

Principal Investigators

  • Diansan Su, Dr. · Department of Anesthesiology Renji Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2022-09-01
Completion
2023-01-01

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05030870 on ClinicalTrials.gov