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Clinical Trials/PACTR201806003371275
PACTR201806003371275Not yet recruiting未知

Efficacy of Two CAD CAM Oral Appliances for Treatment of Obstructive Sleep Apnea Hypopnea Syndrome (Randomized Controlled Clinical Trial)

Faculty of Dentistry, Alexandria University.0 sites20 target enrollmentStarted: May 4, 2018Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Not yet recruiting
Sponsor
Enrollment
20

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 Year(s) to 50 Year(s) (—)
Sex
All

Inclusion Criteria

  • All patients had successfully completed all night polysomnography that demonstrate an OSA disorder.
  • Each patient had an apneic hypopneic index (AHI) score greater than or equal to 15 events per hour of sleep.
  • All patients had adequate nasal airflow capacity as determined by a qualified otolarygologist.
  • All patients had at least 7 mm of protrusive jaw movement from the position of maximum intercuspation. (measured by flexible ruler)

Exclusion Criteria

  • Central sleep apnea events more than two or three per hour.
  • Retro-palatal obstructions as confirmed by nasoendoscopy.
  • More than one missing tooth per quadrant, excluding third molars (fixed bridges were not considered missing).
  • History of alcohol or narcotic or psychoactive medications.
  • Serious nasal passage obstructions or allergies.

Investigators

Sponsor
Faculty of Dentistry, Alexandria University.

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