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

The CryoICE™ Cryoanalgesia Registry for Pain Management in Post-cardiothoracic Surgery Via Cryoablation of the Intercostal Nerves

Who can join

Ages 12 and older · All sexes

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

About the study

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.

What is being tested

• AtriCure Cryo Nerve Block (cryoNB) Device Family (device)

Sponsor: AtriCure, Inc. · Participants: 5,000 · Started: Jun 29, 2018

Contact the study team

• Elizabeth Menard · Phone: 8327120715
• Laura O'Brien, PhD · Phone: 763-310-6151

Official record on ClinicalTrials.gov — NCT05110989

Locations in the U.S.

Conditions

• Pain After Surgery

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.