RECRUITING

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

Description

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

Conditions

AmputationAmputation of Lower LimbAmputation of Upper LimbAmputation, Limb LossAmputation, Traumatic/SurgeryCryo Analgesia
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Related Conditions:

AmputationAmputation of Lower LimbAmputation of Upper LimbAmputation, Limb LossAmputation, Traumatic/SurgeryCryo Analgesia

Study Overview

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Study Details

Study overview

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

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

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

Condition
Amputation
Intervention / Treatment

-

Contacts and Locations

Manchester

Elliot Hospital, Manchester, New Hampshire, United States, 03101

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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.
  • * 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.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

AtriCure, Inc.,

Study Record Dates

2035-04