A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves
ConditionPost Operative Pain
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age12+
SponsorAtriCure, Inc.
About this trial
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
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- AtriCure Cryo Nerve Block (cryoNB) Device Family
Treatment groups
No treatment groups listed
Locations
11Austria
Medical University of Vienna Vienna Austria
Belgium
UZ Leuven Leuven Belgium
Germany
University of Heidelberg Heidelberg Germany
United Kingdom
University Hospitals Leicester NHS Trust Leicester United Kingdom
Sponsors and collaborators
AtriCure, Inc.
Lead sponsor
Source ClinicalTrials.gov