Pure Global
NCT06284109

Preoperative (Pre-amputation) Cryoanalgesia to Improve Post-amputation Phantom Limb Pain

Preoperative (Pre-amputation) Cryoanalgesia to Improve Post-amputation Phantom Limb Pain, General Physical and Emotional Disability, and Opioid Consumption: a Randomized Pilot Trial
The Cleveland Clinic·ClinicalTrials.gov·device·Device trialNot yet recruiting
View on ClinicalTrials.gov →
Study focus
Disease/Condition
Postoperative Pain
Drug/Device/Intervention
Cryoanalgesia
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
The Cleveland Clinic
Timeline & enrollment
Phase
N/A
Start date
Apr 01, 2024
End date
Dec 31, 2024
Enrollment
20 participants
Primary outcome

Phantom limb pain score

Summary

Investigators will evaluate preamputation cryoanalgesia on pain, mobility, opioid use and
 general physical and emotional disability using a pilot randomized trial design, to explore
 the amount and variability of improvement on those outcomes and to investigate the
 potentiality of conducting a future larger randomized controlled trial, which the
 investigators will assess quantitatively the benefits of cryoanalgesia.

ICD-10 classifications
Acute painPostoperative intestinal obstructionPain, unspecifiedDuring surgical operationDuring surgical operation
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06284109
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06284109 through Pure Global AI's free database. This phase not specified trial is sponsored by The Cleveland Clinic and is currently Not yet recruiting. The study focuses on Postoperative Pain. Target enrollment is 20 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.