Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07307560

High-Flow Nasal Cannula for Preventing Hypoxia During Sedated Endoscopy in High-Risk Obstructive Sleep Apnea Patients

High-Flow Nasal Cannula for Preventing Hypoxia During Sedated Endoscopy in High-Risk Obstructive Sleep Apnea Patients: A Multicenter Randomized Trial

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

Summary

Hypoxia represents the most frequent adverse event during propofol-sedated gastrointestinal endoscopy. The STOP-BANG questionnaire serves as a widely adopted, straightforward tool for screening obstructive sleep apnea (OSA) risk, with a score ≥5 identifying high-risk OSA patients who are particularly susceptible to hypoxia under sedation. Although preliminary research from our team suggests that High-Flow Nasal Cannula (HFNC) may lower the incidence of hypoxemia, evidence remains limited and inconsistent in studies specifically targeting high-risk OSA populations. Therefore, this multicenter randomized controlled trial aims to evaluate whether HFNC can effectively reduce the occurrence of hypoxia during sedated gastrointestinal endoscopy in patients identified as high-risk for OSA.

Conditions

Interventions

TypeNameDescription
DEVICEHigh-flow nasal cannula GroupUsing High-flow nasal cannula oxygenation
DEVICERegular Nasal CannulaUsing regular nasal cannula for oxygenation

Timeline

Start date
2025-12-21
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2025-12-29
Last updated
2026-02-27

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07307560. Inclusion in this directory is not an endorsement.