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
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