RecruitingNCT05110989

A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves

The CryoICE™ Cryoanalgesia Registry for Pain Management in Post-cardiothoracic Surgery Via Cryoablation of the Intercostal Nerves

Sponsor

AtriCure, Inc.

Enrollment

5,000 participants

Start Date

Jun 29, 2018

Study Type

OBSERVATIONAL

Conditions

Post Operative Pain

Summary

This is a retrospective and prospective, multicenter, observational patient registry to record outcomes from patients undergoing cryoablation of the intercostal nerves (cryoanalgesia) for post-operative pain management.

Eligibility

Min Age: 12 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying AtriCure Cryo Nerve Block (cryoNB) Device Family for people with post operative pain. The study is currently recruiting participants at 11 locations. People eligible for this study include aged 12 Years and older.

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

DEVICEAtriCure Cryo Nerve Block (cryoNB) Device Family

Use of Atricure Cryo Nerve Block Device Family to generate cryoanalgesia for the management of post operative pain.

Locations(11)

Baptist MD Anderson Cancer Center

Jacksonville, Florida, United States

AdventHealth

Orlando, Florida, United States

Luminis Health Anne Arundel Medical Center

Annapolis, Maryland, United States

St. Luke's Hospital of Kansas City

Kansas City, Missouri, United States

Elliot Hospital

Manchester, New Hampshire, United States

The Christ Hospital

Cincinnati, Ohio, United States

Baylor College of Medicine

Houston, Texas, United States

Medical University of Vienna

Vienna, Austria

UZ Leuven

Leuven, Belgium

University of Heidelberg

Heidelberg, Germany

University Hospitals Leicester NHS Trust

Leicester, United Kingdom

View Full Details on ClinicalTrials.gov

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