AtriCure Cryo Nerve Block (cryoNB) Device Family: Use of Atricure Cryo Nerve Block Device Family to generate cryoanalgesia for the management of post operative pain.
Study 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
Sex
ALL
Min age
12 Years
Max age
—
Healthy volunteers
No
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
Primary outcome measure(s)
Efficacy of cryo nerve block to generate cryoanalgesia as post operative pain management — From enrollment to 5 years after date of index procedure Collect pain score to assess the effect of cryoanalgesia effect with a follow up duration of up to 5 years.
Safety of cryo nerve block to generate cryoanalgesia as post operative pain management — From enrollment to 5 years after date of index procedure Collect adverse events occurred during and post operation to assess the safety of the cryo nerve block procedure.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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