Extension Study of Original Protocol AERO C009 for Obstructive Sleep Apnea-hypopnea
Public ClinicalTrials.gov record NCT00849043. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Single Arm, Open-label Extension Study to Evaluate the Long-term Durability of Treatment Response and and Safety of the Provent Professional Sleep Apnea Therapy Device for the Non-invasive Treatment of Obstructive Sleep Apnea-hypopnea
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to evaluate the long-term durability of the treatment and safety of the Provent device for those individuals who were enrolled in the C009 study, were diagnosed with obstructive sleep apnea-hypopnea (OSAH), and were actively using the Provent device.
Study identification
- NCT ID
- NCT00849043
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 65 participants
Conditions and interventions
Interventions
Not listed
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Feb 2009 (Type not available)
- Primary completion
- Aug 2010 (Actual)
- Completion
- Oct 2010 (Actual)
- Last update posted
- Jan 26, 2011
2009 – 2010
United States locations
- U.S. sites
- 13
- U.S. states
- 11
- U.S. cities
- 13
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Gaylord Sleep Medicine Research | Wallingford | Connecticut | 06492 | — |
| University of Florida Health Science Center | Gainesville | Florida | 32610-0225 | — |
| Sleep Disorders Center of Georgia | Atlanta | Georgia | 30342 | — |
| Suburban Lung Associates | Elk Grove Village | Illinois | 60007 | — |
| Kentucky Research Group | Louisville | Kentucky | 40217 | — |
| Sleep HealthCenters | Brighton | Massachusetts | 02135 | — |
| Wayne State University Harper Univ. Hospital | Detroit | Michigan | 48201 | — |
| Borgess Research | Kalamazoo | Michigan | 49024 | — |
| Mayo Clinic | Rochester | Minnesota | 55905 | — |
| St. Luke's Hospital Sleep Medicine & Research Center | Chesterfield | Missouri | 63001 | — |
| The Corvallis Clinic | Corvallis | Oregon | 97330 | — |
| Sleep Medicine Associates of Texas | Dallas | Texas | 75231 | — |
| Sleep Therapy and Research Center | San Antonio | Texas | 07829 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00849043, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jan 26, 2011 · Synced Oct 19, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT00849043 live on ClinicalTrials.gov.