C-LIFT Efficacy in Patients With Obstructive Sleep Apnea

Sex: All

Ages: 18 Years – N/A

Healthy volunteers: No

Phase: NA

Enrollment: 10

Sponsor: Ata Murat Kaynar

Location: The Center for Sleep and Cardiovascular Outcomes Research (C-SCOR) Sleep Laboratory Pittsburgh Pennsylvania

Summary

The goal of this clinical trial is to evaluate the efficacy of the C-Lift Device as a non-invasive treatment for Sleep Disordered Breathing (SDB) within the population of adults diagnosed with moderate to severe Obstructive Sleep Apnea (OSA), who are not currently being treated with a Continuous Positive Airway Pressure (CPAP) device or other intervention. This study aims to answer 2 main questions: "Will C-Lift demonstrate a qualitative improvement in a participant's perception/description of their sleep-quality?" And, "Will wearing the C-Lift Device overnight show a quantitative improvement in a participant's oxygen saturation?"

Eligibility Criteria

Inclusion Criteria: * Diagnosis of moderate to severe OSA (≥16 AHI events per hour) * Previously failed/refused CPAP * Not currently/actively participating in treatment for OSA Exclusion Criteria: * Diagnosis of mild OSA (AHI\

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07807124). StuddyBuddy aggregates publicly available trial information.