Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Day of amputation procedure
Participants undergo cryoablation using AtriCure devices during their extremity amputation procedure.
1 procedure visit (in-person)
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
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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