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Clinical Trial of the Cryosa System for the Treatment of Obstructive Sleep Apnea (OASIS)

NCT07720219 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2026-07-22

No results posted yet for this study

Summary

The objective of this study is to evaluate the safety and effectiveness of the Cryosa System when used as intended to perform the Cryosa Procedure.

Conditions

  • Obstructive Sleep Apnea (OSA)
  • Sleep Apnea - Obstructive
  • OSA

Interventions

DEVICE

Cryosa Procedure

Cryotherapy

Sponsors & Collaborators

  • Cryosa, Inc.

    lead INDUSTRY

Principal Investigators

  • B. Tucker Woodson, MD · Medical College Wisconsin

  • Michael J Hutz, MD · Rush University Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-10-31
Primary Completion
2029-05-31
Completion
2029-11-30
FDA Device
Yes

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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 NCT07720219 on ClinicalTrials.gov