New sedation combo could speed up endoscopy recovery
NCT ID NCT07423676
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a combination of ketamine and dexmedetomidine (Ketodex) works faster and safer than the usual propofol-midazolam for sedation during upper GI endoscopy. Fifty-two adults aged 21–60 will be enrolled. Researchers will measure how quickly patients reach the right sedation level, how fast they recover, and any side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ketamine and dexmedetomidine (Ketodex) compared to propofol and midazolam
- What this could lead to
- If Ketodex works better, it could offer a faster, safer sedation option for routine GI endoscopy.
- What could go wrong
- This is a small, early-stage trial with only 52 participants. Results may not apply to all patients, and side effects like nausea or blood pressure changes are possible.
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.
- Participants
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About 52 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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May 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients not more than 60 years old with BMI \< 35 kg/m2
- Ages
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21 to 60 years
- Sex
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Anyone
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 * Patient acceptance * Adults aged 21-60 years. * Both sexes * BMI\<35 kg/m2 * ASA physical status :I\& II * Patients Undergoing Gastrointestinal endoscopy * Duration \<30mintues Exclusion Criteria: * • Known allergy to any of the study drugs * Unstable Cardiovascular disease * Moderate to severe respiratory diseases
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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