Home › NCT06908538

Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain

Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain (VANISH)

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* Patients who have or will have an amputation procedure;
* Patients who are willing and capable of providing informed consent;
* Patients whose age is 18 years or above, or of legal age to give informed consent specific to state and national law.

Exclusion Criteria:

* Women of childbearing potential who are, or plan to become, pregnant during the time of the study;
* Other medical, social, or psychological conditions that in the opinion of the Investigator precludes the subject from appropriate consent or adherence to the protocol.

About the study

The goal of this Registry is to see how the device is used when freezing nerves during an amputation procedure.

What is being tested

• cryoablation (device)

Sponsor: AtriCure, Inc. · Participants: 2,000 · Started: Apr 1, 2025

Contact the study team

• Senior Registry Specialist · Phone: 1 (866) 349-2342

Official record on ClinicalTrials.gov — NCT06908538

Locations in the U.S.

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