Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05783245

Effect of Cooling Therapy for Post-Operative Pain in Open Carpal Tunnel Release

Led by University of Chicago · Updated on 2026-02-05

128

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the clinical differences between continuous cooling therapy and traditional ice therapy for managing post-operative pain following open carpal tunnel release (CTR) surgery. CTR surgery is common in the U.S., with over 400,000 procedures yearly, and effective pain control is essential. While ice is commonly used after CTR surgery, there is limited and conflicting data on the benefits of continuous cooling devices like the Polar Care machine compared to traditional icing methods. Participants will be randomly assigned to one of two groups: one using the Polar Care continuous cooling machine and the other using standard commercial reusable ice packs. Both groups are instructed to use their assigned therapy as often as possible, with at least three 15-minute sessions per day for the first three days after surgery. No single icing session should exceed 30 minutes. During the study, participants will complete online questionnaires to assess pain levels using the Visual Analog Scale (VAS) at 3 days after surgery and the Disabilities of the Arm, Shoulder, and Hand questionnaire at 1 week. Researchers will monitor pain control effectiveness and any post-operative complications. The study is sponsored by the University of Chicago and includes adult participants undergoing open CTR surgery.

CONDITIONS

Brief Title

Effect of Cooling Therapy for Post-Operative Pain in Open Carpal Tunnel Release

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 or older
  • Scheduled for open carpal tunnel release surgery
  • Able and willing to complete online questionnaires
Not Eligible

You will not qualify if you...

  • Prior carpal tunnel surgery on the same arm
  • Additional procedures planned on either arm
  • Current use of opioid or narcotic pain medications

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - 3 days

Participants undergo open carpal tunnel release surgery followed by post-operative pain management using either continuous cooling therapy with the PolarCare machine or standard ice packs.

Daily use of cooling therapy with a minimum of three 15-minute sessions per day

Post-operative Follow-up

Duration - 1 week

Participants complete pain and disability assessments to evaluate recovery and treatment effectiveness.

Online questionnaires completed after surgery

Trial Site Locations

Total: 1 location

1

University of Chicago Medicine

Chicago, Illinois, United States, 60637

Actively Recruiting

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Research Team

P

Patrick Nelson, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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