RecruitingNot ApplicableNCT04572503
Modified Anterior Palatoplasty In Obstructive Sleep Apnea Syndrome
Barbed Suture Modified Anterior Palatoplasty In Management of Mild and Moderate Obstructive Sleep Apnea Syndrome
Sponsor
Benha University
Enrollment
20 participants
Start Date
Oct 7, 2020
Study Type
INTERVENTIONAL
Conditions
Summary
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).
Eligibility
Min Age: 18 Years
Inclusion Criteria3
- 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 Criteria7
- Patients diagnosed with sever OSAS (AHI more than 30)
- The main site of obstruction at retrolingual level or multilevel obstruction.
- Contraindication of surgery (e.g. cardiovascular problems and bleeding tendency).
- Patients with significant craniofacial anomalies affecting airway.
- Patients with BMI>40 kg/m2.
- Patients unfit for general anesthesia.
- History of previous velopharyngeal or lingual surgeries.
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Interventions
PROCEDUREBarbed Suture Modified Anterior Palatoplasty
Barbed Suture Modified Anterior Palatoplasty using single resorbable polydioxanone barbed bidirectional size 0 monofilament suture
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04572503
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