Can adding ketamine to propofol improve sleep apnea scans?
NCT ID NCT04452383
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers test whether adding ketamine to propofol improves sedation for drug-induced sleep endoscopy in adults with obstructive sleep apnea. The procedure lets doctors see where the airway collapses during sleep. Thirty adults receive either propofol alone or propofol plus ketamine. The team measures how often the procedure is completed successfully and how quickly sufficient sedation is reached.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ketamine added to propofol
- What this could lead to
- If adding ketamine helps, doctors could get clearer pictures of airway blockages during sleep endoscopy, which may guide better treatment choices for sleep apnea.
- What could go wrong
- This is a small, single-center study of 30 people, so results may not apply broadly. Ketamine can cause hallucinations or blood pressure changes, and the combination might not work better than propofol alone.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
30 people
The number who actually took part.
- Started
-
Jul 2024
- Finished
-
Dec 2025
- Lead sponsor
-
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.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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 * Age \> 18 years old. * American society of anesthesiologists (ASA) physical status I or II. I / II Exclusion Criteria: * patient refusal * American society of anesthesiologists (ASA) physical status \> III * known or suspected allergy to the studied drugs or its components, allergy to eggs or soy beans * morbid obesity * patients with moderate to severe chronic obstructive pulmonary disease or uncontrolled asthma, congestive e heart failure ,seizures ,or cerebrovascular disease * pregnancy
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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
-
zagazig University
Zagazig, Sarkia, 44519, Egypt
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