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Extension Study of Original Protocol AERO C009 for Obstructive Sleep Apnea-hypopnea

NCT00849043 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2011-01-26

No results posted yet for this study

Summary

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.

Conditions

Sponsors & Collaborators

  • Ventus Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Meir Kryger, MD · Gaylord Sleep Medicine Research

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2010-08-31
Completion
2010-10-31

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00849043 on ClinicalTrials.gov