Actively Recruiting

Age: 18Years +
All Genders
ID06908538

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

Led by AtriCure, Inc. · Updated on 2026-01-07

2000

Participants Needed

4

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational registry studies how AtriCure devices are used to freeze nerves during limb amputation procedures. The focus is on gathering real-world safety and performance information about cryoablation, a technique that applies extreme cold to nerves to temporarily block sensation, which may help manage post-operative and phantom limb pain. Participants include adults who have had or will have an amputation. The registry observes patients undergoing amputation procedures where cryoablation devices are used on nerves. Cryoablation involves applying very cold temperatures to nerves to cause reversible nerve injury, blocking nerve signals temporarily until nerve function recovers over weeks to months. The study collects data during and after the procedure without assigning specific treatments. Participants provide informed consent and are followed for at least 30 days to assess safety and how the device performs. Researchers collect information on nerve freezing during the amputation, monitor outcomes related to pain, and evaluate any side effects or complications. Data collection focuses on real-world use, with no experimental treatment assignments, and participation duration varies based on the timing of the procedure and follow-up.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who have or will have an amputation procedure
  • Patients who are willing and capable of providing informed consent
  • Patients aged 18 years or older, or of legal age to give informed consent according to local law
Not Eligible

You will not qualify if you...

  • Women who are of childbearing potential and are pregnant or plan to become pregnant during the study
  • Patients with medical, social, or psychological conditions that prevent giving proper consent or following the study protocol, as determined by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - Day of amputation procedure

Participants undergo cryoablation using AtriCure devices during their extremity amputation procedure.

1 procedure visit (in-person)

Post-operative Follow-up

Duration - 30 days

Participants are monitored for safety and device performance after the amputation and cryoablation procedure.

Approximately 1 to 2 follow-up visits

Trial Site Locations

Total: 4 locations

1

Berkshire Medical Center

Pittsfield, Massachusetts, United States, 01201

Actively Recruiting

2

Elliot Hospital

Manchester, New Hampshire, United States, 03101

Actively Recruiting

3

NYU Langone Health

New York, New York, United States, 10017

Actively Recruiting

4

Medical College of Wisconsin/Froedtert Hospital

Milwaukee, Wisconsin, United States, 53226

Actively Recruiting

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Research Team

S

Senior Registry Specialist

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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