RecruitingNot ApplicableNCT07516327

Cold and Compression After Rotator Cuff Repair (RCR)

Cold and Compression After Rotator Cuff Repair or Arthroscopic Rotator Cuff Repair Pain Attenuation: A Randomized, Controlled Trial


Sponsor

Ochsner Health System

Enrollment

90 participants

Start Date

Mar 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to compare pain score (Patient-Reported Outcomes Measurement Information System: PROMIS NRS Pain Subscale) between the control and cold/compression groups pre-surgically, daily after surgery for 14 days, then weekly after surgery for 3 months, and at 6 months post-surgery.


Eligibility

Min Age: 35 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Cold and Compression and SOC (Standard of care) for people with high-grade partial or full thickness rotator cuff tears. The study is currently recruiting participants at 1 location. People eligible for this study include aged 35 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERSOC (Standard of care)

Patients enrolled in this arm will be discharged with 28 hydrocodone/APAP 7.5 mg pills taken every 6 hours as needed (or its MME equivalent), 1 identical refill if patient calls, and cold therapy (bag of ice or gel pack) Other Name:

DEVICECold and Compression

External mechanical compression therapy (e.g., compression stockings) has been shown to reduce swelling and risk of deep vein thrombosis in the lower limbs following TKA.12,13 Combining advanced cryotherapy (continuous circulating cold flow) and dynamic compression may offer added benefits than either traditional cryotherapy (e.g., cold packs) or compression (e.g., stockings) alone.


Locations(1)

Ochsner Medical Center - Kenner

Kenner, Louisiana, United States

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NCT07516327