Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07012772

COMBO Endoscopy Oropharyngeal Airway in Sedated Endoscopic Retrograde Cholangiopancreatography for Patients

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Zhejiang University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Hypoxia represents the prevailing adverse occurrence during the sedation of patients undergoing Endoscopic Retrograde Cholangiopancreatography (ERCP) with propofol. 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 assess the efficacy of the COMBO Endoscopy Oropharyngeal Airway in reducing the incidence of hypoxia in patients undergoing ERCP under sedation.

Conditions

Interventions

TypeNameDescription
DEVICEThe COMBO Endoscopy Oropharyngeal AirwayUsing the COMBO Endoscopy Oropharyngeal Airway for oxygenation.

Timeline

Start date
2025-06-12
Primary completion
2025-09-30
Completion
2025-12-31
First posted
2025-06-10
Last updated
2025-06-24

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07012772. Inclusion in this directory is not an endorsement.