Measuring Effectiveness in Sleep Apnea Surgery
Completed · Not applicable
Conditions studied: Obstructive Sleep Apnea
In brief
The goal of this research is to improve our understanding of the effectiveness of surgical OSA treatment by evaluating its impact on these health-related and functional outcomes and comparing these effects to the changes in respiratory physiology achieved after surgery. To achieve this goal, we will examine key health-related (C-reactive protein, homocysteine, leptin, the homeostasis model of insulin resistance, and heart rate variability) and functional (sleep-related quality of life and vigilance) measures among a surgical group of OSA patients who do not tolerate non-surgical treatment (positive airway pressure, PAP) and a comparison group of matched OSA patients who tolerate PAP.
Key facts
- Study ID
- NCT00518128
- Run by
- University of California, San Francisco
- People needed
- 60
- Starts
- 2007-07-01
- Expected to finish
- 2011-06-01
- Last updated by the study team
- 2012-05-22
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may not qualify if…
- Pregnant women
- Primary snoring or mild OSA (apnea-hypopnea index < 15)
- Known neurologic, cardiac, hepatic, or renal disorder
- Acute illness or infection
- Co-existing sleep disorder other than primary snoring
- Unable to fast overnight prior to blood draw
Where it is running
- UCSF Department of Otolaryngology - Head and Neck Surgery — San Francisco, California, United States
Full record on ClinicalTrials.gov
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