Combination COMBO Endoscopy Oropharyngeal Airway With High-Flow Nasal Cannula Oxygenation in Sedated Gastrointestinal Endoscopy for Obese Patients
1 other identifier
interventional
50
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_2
Started Feb 2025
Shorter than P25 for phase_2
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 1, 2025
CompletedStudy Start
First participant enrolled
February 4, 2025
CompletedFirst Posted
Study publicly available on registry
February 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 4, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 4, 2025
CompletedJune 25, 2025
March 1, 2025
4 months
February 1, 2025
June 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The incidence of hypoxia
75% ≤ SpO2 \< 90% for \<60 s
Patients will be followed for the duration of hospital stay, an expected average about 2 hours
Secondary Outcomes (2)
The incidence of subclinical respiratory depression
Patients will be followed for the duration of hospital stay, an expected average about 2 hours
The incidence of severe hypoxia
Patients will be followed for the duration of hospital stay, an expected average about 2 hours
Other Outcomes (1)
The incidence of other adverse events
Patients will be followed for the duration of hospital stay, an expected average about 2 hours
Study Arms (1)
the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation
EXPERIMENTALIn this group, patients use the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation.
Interventions
Using the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation in Sedated Gastrointestinal Endoscopy for Obese Patients
Eligibility Criteria
You may qualify if:
- Age 18≤ Age ≤70.
- BMI ≥ 35 kg/m².
- The ASA classification ranges from I to III.
- Patients have signed the informed consent form.
- Patients undergoing gastroendoscopy and colonoscopy procedure.
- The estimated duration of the procedure does not exceed 45 minutes.
You may not qualify if:
- Patients who exhibit contraindications to oropharyngeal airway ventilation, such as coagulation disorders, a predisposition to oral and nasal bleeding, mucosal damage, or anatomical constraints impeding oropharyngeal channel placement.
- Severe cardiac insufficiency, defined as a maximal exercise capacity of less than 4 metabolic equivalents (METs).
- Profound renal insufficiency necessitating preoperative dialysis.
- A confirmed severe liver dysfunction.
- Patients diagnosed with chronic obstructive pulmonary disease (COPD) or those presently experiencing other acute and chronic pulmonary conditions necessitating prolonged or intermittent oxygen therapy.
- Elevated intracranial pressure.
- Upper respiratory tract infections, encompassing the oral, nasal, and pharyngeal regions.
- Fever, defined as a core body temperature exceeding 37.5 degrees Celsius.
- Pregnancy or lactation.
- Hypersensitivity reactions to sedatives like propofol or medical equipment such as adhesive tape.
- Urgent surgical intervention.
- Polytrauma.
- Peripheral oxygen saturation (SpO2) levels below 95% while breathing room air preoperatively.
- BMI\<35 kg/m².
- Patients with a documented history of substance abuse, specifically drugs and/or alcohol, within the two years preceding the commencement of the screening period. Substance abuse in this context is defined as consuming more than three standard alcoholic beverages daily, roughly equivalent to 10g of alcohol or 50g of Chinese Baijiu.
- +2 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The First Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, 310000, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chair of the Department of Anesthesiology
Study Record Dates
First Submitted
February 1, 2025
First Posted
February 6, 2025
Study Start
February 4, 2025
Primary Completion
June 4, 2025
Study Completion
June 4, 2025
Last Updated
June 25, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share