COMBO Endoscopy Oropharyngeal Airway in Sedated Endoscopic Retrograde Cholangiopancreatography for Patients

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 2
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years;

• The ASA classification ranges from I to III.

• Patients have signed the informed consent form.

• Patients scheduled to undergo sedated ERCP examination;

• The estimated duration of the procedure does not exceed 45 minutes.

Locations
Other Locations
China
he First Affiliated Hospital, Zhejiang University School of Medicine
RECRUITING
Hangzhou
The First Affiliated Hospital,Zhejiang University School of Medicine
RECRUITING
Hangzhou
Contact Information
Primary
DiSan Head of Anesthesiology, PhD
184872238@qq.com
86+18616514088
Backup
Lianjuan Sun, Master
sunlianjuan26@163.com
+8618257152767
Time Frame
Start Date: 2025-06-12
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 50
Treatments
Experimental: The COMBO Endoscopy Oropharyngeal Airway Group
In this group, patients use the COMBO Endoscopy Oropharyngeal Airway for oxygenation.
Sponsors
Leads: Zhejiang University

This content was sourced from clinicaltrials.gov