Cold and Compression After Rotator Cuff Repair (RCR)
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age35+
SponsorOchsner Health System
About this trial
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 criteria
Qualifiers
Aged 35 yr or older
Patient of Drs. Michael Hartman (PI), Ian Elliott, Jay French, or Paul Phillips at Ochsner Kenner scheduled for arthroscopic rotator cuff repair
Will receive outpatient physical therapy at OTW Driftwood for the entire post-op rehabilitation period
English speaking
Disqualifiers
Chronic opioid use
Opioid use within the last 3 months
Diagnosis of inflammatory disease process (i.e., gout, rheumatoid arthritis, systematic lupus erythematosus...)
Discharge to skilled nursing
Trial design
Treatments tested in this trial
- SOC (Standard of care)
- Cold and Compression
Treatment groups
90 Participants
are divided into 2 treatment groupsSponsors and collaborators
Ochsner Health System
Lead sponsor
BREG, Inc
Collaborator
Source ClinicalTrials.gov