NCT06812403

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for phase_2

Timeline
Completed

Started Feb 2025

Shorter than P25 for phase_2

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 1, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

February 4, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

February 6, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 4, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 4, 2025

Completed
Last Updated

June 25, 2025

Status Verified

March 1, 2025

Enrollment Period

4 months

First QC Date

February 1, 2025

Last Update Submit

June 19, 2025

Conditions

Keywords

The COMBO Endoscopy Oropharyngeal AirwayHypoxiaHigh-flow nasal cannula OxygenationsedationGastrointestinal endoscopes

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

EXPERIMENTAL

In this group, patients use the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation.

Device: 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

the COMBO Endoscopy Oropharyngeal Airway with High-Flow Nasal Cannula Oxygenation

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

HypoxiaEsophageal NeoplasmsStomach NeoplasmsColonic Polyps

Condition Hierarchy (Ancestors)

Signs and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and SymptomsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsHead and Neck NeoplasmsDigestive System DiseasesEsophageal DiseasesGastrointestinal DiseasesStomach DiseasesIntestinal PolypsPolypsPathological Conditions, Anatomical

Study Design

Study Type
interventional
Phase
phase 2
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: Combined use of the COMBO Endoscopy Oropharyngeal Airway with high-flow nasal Cannula Oxygenation in morbidly obese patients undergoing endoscopy
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

Locations