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

AtriCure

Status: Enrolling

Conditions: Post Operative Pain

Treatments: Device: AtriCure Cryo Nerve Block (cryoNB) Device Family

Study type: Observational

Funder types: Industry

Identifiers

NCT05110989

REDUCE2018

Details and patient eligibility

About

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.

Enrollment: 5,000 estimated patients

Sex: All

Ages: 12+ years old

Volunteers: No Healthy Volunteers

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