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Completed Phase 1Phase 2 Interventional Results available

Sleep Apnea Treatment With Expiratory Resistance(Provent™)

NCT01061476
Conditions
Sleep Apnea, Obstructive
Interventions
Treatment sleep study (Provent™ device used), Baseline sleep study (No device), Physiology sleep study (Provent™ on/off)
Device · Other
Lead sponsor
Johns Hopkins University
Other
Eligibility
21 Years and older
Enrollment
12 participants
Healthy volunteers
Healthy volunteers not accepted
Timeline
2010 – 2011
U.S. locations
1
States / cities
Baltimore, Maryland