NCT06283095RecruitingNot Applicable
Management of Obstructive Sleep Apnea Syndrome by Expansion Palatoplasty
ET Zarief1 site in 1 country30 target enrollmentStarted: November 1, 2023Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Evaluation the outcome of expansion palatoplasty in management of OSAS.
Study Overview
Brief Summary
The study will be conducted to evaluate the outcome of expansion palatoplasty in management of OSAS.
Detailed Description
Expansion palatopladty will be conducted on patients with obstructive sleep apnea patients to evaluate the outcome.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Adult patients.
- •Body mass index < 30 kg/m2 (weight /height in m2)
- •Mild to moderate OSAS
- •Sagittal collapse of the lateral pharyngeal walls proved by Drug induced sleep endoscopy (DISE).
Exclusion Criteria
- •• Refusing enrollment into the study.
- •Pregnant women.
- •Refusing the surgery
- •Contraindication to anaesthesia
- •Patients with multilevel of obstruction.
- •Serious psychiatric, neurological and cardiopulmonary (COPD or corpulmonale) diseases.
- •Uncorrected hypothyroidism.
- •Severe OSAS.
- •Craniofacial anamolies.
- •Central& mixed apnea
- •Morbid obesity.
Arms & Interventions
study group
Experimental
we will do expansion palatoplasty
Intervention: expansion palatoplasty (Procedure)
Outcomes
Primary Outcomes
Evaluation the outcome of expansion palatoplasty in management of OSAS.
Time Frame: Six months
Polysomngrophy
Secondary Outcomes
- Expansion palatoplasty in Obstructive sleep apnea patients(Six months)
Investigators
ET Zarief
Principle investigator
Assiut University
Study Sites (1)
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