Laughing gas may speed recovery after colonoscopy
NCT ID NCT05396144
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if adding nitrous oxide (laughing gas) to standard sedation during GI endoscopy (like colonoscopy) could reduce side effects such as fatigue, mental fogginess, and nausea after the procedure. The study was designed for adults 18 and older undergoing these procedures. However, the study was withdrawn before enrolling any participants, so no results are available.
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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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Started
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May 2024
- Expected to finish
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Aug 2025
An estimate. End dates often move.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Non-pregnant patients age 18 and older * Patient's presenting for upper endoscopy or colonoscopy under endoscopist- directed nurse sedation. * Patient is willing and able to consent and comply with study procedures. Exclusion Criteria: * Age \<18 * Potentially vulnerable subjects including, homeless people, pregnant females, employees and students. * Participation in another investigational study that may directly or indirectly affect the results of this study within 30 days prior to the initial visit * Allergy to the proposed anesthetic agents (e.g. nitrous oxide, midazolam, fentanyl, diphenhydramine)
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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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Stanford University Hospital
Stanford, California, 94305, United States
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Other studies related to the condition(s) this trial covers.
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