Management of Obstructive Sleep Apnea Syndrome by Expansion Palatoplasty
ConditionObstructive Sleep Apnea of Adult
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorET Zarief
About this trial
The study will be conducted to evaluate the outcome of expansion palatoplasty in management of OSAS.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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).
Disqualifiers
• Refusing enrollment into the study.
Pregnant women.
Refusing the surgery
Contraindication to anaesthesia
Trial design
Design model
Single group
Treatments tested in this trial
expansion palatoplasty
Procedure/Surgerysurgical procedure
Treatment groups
30 Participants
are divided into 1 treatment groupGroup A: study groupExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Evaluation the outcome of expansion palatoplasty in management of OSAS.
Polysomngrophy
Time frame
Six monthsSecondary outcomes
1
Expansion palatoplasty in Obstructive sleep apnea patients
Drug induced sleep endoscopy
Time frame
Six monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
ET Zarief
Lead sponsor
Assiut University
Sponsor institution
Source ClinicalTrials.gov