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NCT05110989Recruiting

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

AtriCure, Inc.

Start Date

6/29/2018

Completion Date

1/1/2040

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 Criteria

Age Range: 12 years to No maximum

Inclusion Criteria: 1. Patients whose age is 12 years or above, and are able to give informed consent/assent specific to state and national law. 2. Patients have been scheduled by physician(s) to undergo or have undergone cryoablation of the intercostal nerves utilizing at least one AtriCure device or are similar patients treated without the use of cryoablation Exclusion Criteria: 1. Patient is enrolled in a concurrent trial that may impact the treatment offered by the registry devices. 2. Patient with exclusion criteria required by local governance. 3. Women of childbearing potential who are, or plan to become, pregnant during the time of the study

Interventions

DEVICE

AtriCure Cryo Nerve Block (cryoNB) Device Family

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Conditions

Post Operative Pain

Locations

Baptist MD Anderson Cancer Center

Jacksonville, Florida 32207

United States

AdventHealth

Orlando, Florida 32803

United States

Luminis Health Anne Arundel Medical Center

Annapolis, Maryland 21401

United States

St. Luke's Hospital of Kansas City

Kansas City, Missouri 64111

United States

Elliot Hospital

Manchester, New Hampshire 03101

United States

The Christ Hospital

Cincinnati, Ohio 45219

United States

Baylor College of Medicine

Houston, Texas 77030

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