Trials / Completed
CompletedNCT06812403
Combination COMBO Endoscopy Oropharyngeal Airway With High-Flow Nasal Cannula Oxygenation in Sedated Gastrointestinal Endoscopy for Obese Patients
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Zhejiang University · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Hypoxia is the most common adverse event during propofol sedation for gastrointestinal endoscopy, particularly in obese patients. A recent innovation in this domain is the COMBO Endoscopy Oropharyngeal Airway-a multifaceted device that encompasses capnography monitoring, bite block , oxygenation support, and oropharyngeal airway management. This device has been purposefully designed to cater to the unique requirements of endoscopic procedures. The principal objective of this study is to evaluate the efficacy of the COMBO Endoscopy Oropharyngeal Airway in combination with High-Flow Nasal Cannula Oxygenation for reducing the incidence of hypoxia in obese patients undergoing gastrointestinal endoscopy under sedation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation | Using the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation in Sedated Gastrointestinal Endoscopy for Obese Patients |
Timeline
- Start date
- 2025-02-04
- Primary completion
- 2025-06-04
- Completion
- 2025-06-04
- First posted
- 2025-02-06
- Last updated
- 2025-06-25
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06812403. Inclusion in this directory is not an endorsement.