Modified Anterior Palatoplasty In Obstructive Sleep Apnea Syndrome
Recruiting
N/A
Interventional Study
Obstructive Sleep Apnea
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 20 (estimated)
- Sponsor
- Benha University · Other
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About This Trial
The aim of this study is to evaluate the effectiveness of barbed suture modification of anterior palatoplasty in the treatment of patients with retropalatal mild to moderate obstructive sleep apnea syndrome (OSAS).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with mild to moderate obstructive sleep apnea syndrome.
* Patients diagnosed with mild (AHI 5 to15) and moderate (AHI 16 to 30) OSAS with only retropalatal collapses
* Patients who are noncompliant with Continuous positive airway pressure (CPAP).
Exclusion Criteria:
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Contacts