Sleep apnea diagnosis: can a sedated scope outperform a standard office test?
NCT ID NCT07723417
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This study compares two techniques for evaluating upper airway collapse in people with obstructive sleep apnea: the standard office-based Müller's maneuver and drug-induced sleep endoscopy (DISE), which is performed under light sedation. The goal is to see whether DISE provides more accurate information about the location and pattern of airway blockage. Thirty adults with sleep apnea will undergo both procedures, and the findings will be compared to determine which method better guides treatment decisions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Drug-Induced Sleep Endoscopy (DISE) and Müller's maneuver
- What this could lead to
- If DISE proves more accurate than Müller's maneuver, it could become the preferred method for guiding surgical and device treatments in obstructive sleep apnea.
- What could go wrong
- This is a small, early-stage comparison study with only 30 participants. DISE requires sedation, which carries its own risks, and results may not apply to all sleep apnea patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
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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30 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Mar 2026
- 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: 1. Age \> 18 years old. 2. Diagnosed as OSAS according to polysomnography and AASM (June 2023). 3. Body mass index \< 40 Exclusion Criteria: 1. Age \< 18 years. 2. Central sleep apnea. 3. Hypoventilation syndromes. 4. Cardiac arrhythmias. 5. ischemic heart disease. 6. Heart failure.
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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
-
Mansoua University Hospital
Al Mansurah, Dakahlia Governorate, 35511, Egypt
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Other studies related to the condition(s) this trial covers.
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