Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04572503

Modified Anterior Palatoplasty In Obstructive Sleep Apnea Syndrome

Led by Benha University · Updated on 2024-08-28

20

Participants Needed

1

Research Sites

281 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

Modified Anterior Palatoplasty In Obstructive Sleep Apnea Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with mild to moderate obstructive sleep apnea syndrome.
  • Patients diagnosed with mild (AHI 5 to 15) and moderate (AHI 16 to 30) OSAS with only retropalatal collapses.
  • Patients who are noncompliant with Continuous positive airway pressure (CPAP).
Not Eligible

You will not qualify if you...

  • Patients diagnosed with severe 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 greater than 40 kg/m2.
  • Patients unfit for general anesthesia.
  • History of previous velopharyngeal or lingual surgeries.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Benha University Hospital, Faculty of Medicine

Banhā, Qalyubia Governorate, Egypt, 13512

Actively Recruiting

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Research Team

A

Abdelrahman A Abdelalim, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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