Purpose of this Study
Data will be collected from your medical records for the 5 years following your amputation procedure.
You may be asked periodically about your pain level and your recovery or asked to complete questionnaires that were not collected as part of your clinical care. This will be done prior to surgery, at discharge, and then between 1-3 months, 6 months, and annually after surgery for 5 years.
Who Can Participate?
Eligibility
Patients scheduled to undergo or who have already undergone amputation where a cryo Nerve Block (CryoNB) device was used.
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No
What is Involved?
Description
This is an observational registry to monitor and record the outcome data when Cryo Nerve Block (CryoNB) devices are used to freeze and temporarily block pain signals of the nerves when amputation procedure is performed.
Locations
Duke University Hospital
Duke Regional Hospital
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
Cryo NerVe Block Extremity AmputatioN RegIStry for post operative and pHantom limb pain
Principal Investigator
Kevin
Southerland
Protocol Number
PRO00120499
NCT ID
NCT06908538
Phase
IV
Enrollment Status
Open to Enrollment