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
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