Phantom Limb Pain Clinical Trials

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

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

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

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
United States
Massachusetts
Berkshire Medical Center
RECRUITING
Pittsfield
New Hampshire
Elliot Hospital
RECRUITING
Manchester
New York
NYU Langone Health
RECRUITING
New York
Wisconsin
Medical College of Wisconsin/Froedtert Hospital
RECRUITING
Milwaukee
Contact Information
Primary
Senior Registry Specialist
CryoNB-registry@atricure.com
1 (866) 349-2342
Time Frame
Start Date: 2025-04-01
Estimated Completion Date: 2035-04
Participants
Target number of participants: 2000
Treatments
Subjects who have or will have an amputation procedure.
The primary objective of this Registry is to capture real-world safety and performance data on AtriCure devices used to cryoablate nerves during an extremity amputation procedure.
Sponsors
Leads: AtriCure, Inc.

This content was sourced from clinicaltrials.gov