A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves
Recruiting now
Conditions studied: Post Operative Pain
In brief
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.
Key facts
- Study ID
- NCT05110989
- Run by
- AtriCure, Inc.
- People needed
- 5000
- Starts
- 2018-06-29
- Expected to finish
- 2040-01-01
- Last updated by the study team
- 2026-06-29
Who can join
Age: 12 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients whose age is 12 years or above, and are able to give informed consent/assent specific to state and national law.
- 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
You may not qualify if…
- Patient is enrolled in a concurrent trial that may impact the treatment offered by the registry devices.
- Patient with exclusion criteria required by local governance.
- Women of childbearing potential who are, or plan to become, pregnant during the time of the study
Where it is running
- University Hospitals Leicester NHS Trust — Leicester, United Kingdom (enrolling)
- AdventHealth — Orlando, Florida, United States (enrolling)
- Luminis Health Anne Arundel Medical Center — Annapolis, Maryland, United States (enrolling)
- Baptist MD Anderson Cancer Center — Jacksonville, Florida, United States (enrolling)
- Elliot Hospital — Manchester, New Hampshire, United States (enrolling)
- The Christ Hospital — Cincinnati, Ohio, United States (enrolling)
- Baylor College of Medicine — Houston, Texas, United States (enrolling)
- Medical University of Vienna — Vienna, Austria (enrolling)
- UZ Leuven — Leuven, Belgium (enrolling)
- University of Heidelberg — Heidelberg, Germany (enrolling)
- St. Luke's Hospital of Kansas City — Kansas City, Missouri, United States
Full record on ClinicalTrials.gov
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