Trials / Completed
CompletedNCT05030870
Capnographic Monitoring in Gastrointestinal Endoscopy for Elderly Patients
Capnographic Monitoring Decrease the Incidence of Hypoxia of the Elderly Patients Undergoing Gastrointestinal Endoscopy Procedure: a Randomized Multicenter Clinical Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 1,800 (actual)
- Sponsor
- RenJi Hospital · Academic / Other
- Sex
- All
- Age
- 65 Years – 79 Years
- Healthy volunteers
- Accepted
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
| Type | Name | Description |
|---|---|---|
| DEVICE | Capnography monitoring | Standard monitoring and capnographic monitoring. |
| DEVICE | Standard monitoring | Standard monitoring but no capnographic monitoring |
Timeline
- Start date
- 2021-09-01
- Primary completion
- 2022-09-01
- Completion
- 2023-01-01
- First posted
- 2021-09-01
- Last updated
- 2024-03-19
Locations
3 sites across 1 country: China
Source: ClinicalTrials.gov record NCT05030870. Inclusion in this directory is not an endorsement.