New oxygen method may prevent dangerous drops during endoscopy
NCT ID NCT06610461
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether giving high-flow nasal oxygen (HFNO) during upper GI endoscopy in high-risk patients (e.g., those with sleep apnea or obesity) reduces the risk of blood oxygen levels falling too low. 180 patients were randomly assigned to receive either HFNO or standard oxygen via face mask or nasal cannula. The goal was to see if HFNO could prevent the need for emergency airway maneuvers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- High-flow nasal oxygen (HFNO) delivered via a device
- What this could lead to
- If it works, this could provide a safer way to give sedation during upper GI endoscopy in high-risk patients, reducing the need for emergency airway procedures.
- What could go wrong
- This is a small, completed study (180 patients) and results may not apply to all settings. The intervention may not significantly reduce oxygen drops or could cause discomfort.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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180 people
The number who actually took part.
- Started
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Sep 2024
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Upper endoscopy (EGD, ERCP, EUC etc.) w/wo colonoscopy expected duration \> 15 min under MAC * one or more of the following: * Diagnosis of sleep apnea * BMI ≥ 30 kg/m2 * Baseline SpO2 \< 96% or Requirement for long-term oxygen therapy * BOSTN score ≥ 2 * BMI ≥ 30 kg/m2 * Observed apnea * Observed loud Snoring * Daytime Tiredness * Neck circumference ≥ 16.5 inches in female, ≥ 17.5 inches in male Exclusion Criteria: * Known Pregnancy * Known Current infection with COVID-19 * Planned general anesthesia
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Anesthesia, Critical Care and Pain Medicine Department at Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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