RecruitingNot ApplicableNCT06008626

Clinical Trial of the Cryosa System for the Treatment of Obstructive Sleep Apnea

Multicenter Pilot Study of the Cryosa System for the Treatment of Obstructive Sleep Apnea

Sponsor

Cryosa, Inc.

Enrollment

25 participants

Start Date

Sep 12, 2023

Study Type

INTERVENTIONAL

Conditions

Obstructive Sleep Apnea of Adult

Summary

This is a prospective, multicenter, non-randomized single-arm safety and performance study to collect data to evaluate the safety of the Cryosa procedure to treat obstructive sleep apnea (OSA) in patients with moderate to severe OSA. The study will also evaluate the chronic performance of the Cryosa system and collect clinical measures for therapy effectiveness that will be used to demonstrate safety and effectiveness in the next clinical study.

Eligibility

Min Age: 22 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Cryosa Procedure for people with obstructive sleep apnea of adult. The study is currently recruiting participants at 9 locations. People eligible for this study include aged 22 Years to 70 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICECryosa Procedure

Cryotherapy

Locations(9)

UCHealth University of Colorado

Aurora, Colorado, United States

University of Miami

Miami, Florida, United States

Rush University Medical Center

Chicago, Illinois, United States

Ochsner Baptist Medical Center

New Orleans, Louisiana, United States

Albany ENT & Allergy Services

Albany, New York, United States

Specialty Physician Associates

Bethlehem, Pennsylvania, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Tennessee Health Sciences Center

Memphis, Tennessee, United States

Houston Methodist Hospital

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06008626

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