CompletedPhase 4NCT00772044
Randomized Study of Provent Versus Sham Device to Treat Obstructive Sleep Apnea
Studying Carnevale syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Ventus Medical, Inc.
- Principal Investigator
- Richard B Berry, M.D.University of Florida
- Intervention
- Provent Professional Sleep Apnea Therapy Device(device)
- Enrollment
- 250 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2008 – 2009
Study locations (17)
- Pulmonary Associates, Glendale, Arizona, United States
- Pulmonary Associates, Phoenix, Arizona, United States
- Stanford Center for Human Sleep Research, Redwood City, California, United States
- Gaylord Sleep Medicine, Wallingford, Connecticut, United States
- University Of Florida College of Medicine, Gainesville, Florida, United States
- Sleep Disorders Center of Georgia, Atlanta, Georgia, United States
- Chicago Sleep Group of Suburban Lung Associates, Elk Grove Village, Illinois, United States
- Kentucky Research Group, Louisville, Kentucky, United States
- Sleep Health Center, Brighton, Massachusetts, United States
- Wayne State University, Detroit, Michigan, United States
- Borgess Research Institute, Kalamazoo, Michigan, United States
- Mayo Clinic, Rochester, Minnesota, United States
- Sleep Medicine and Research Center, Chesterfield, Missouri, United States
- The Corvallis Clinic, Corvallis, Oregon, United States
- SleepMed of South Carolina, Columbia, South Carolina, United States
- +2 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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