About this trial
Effective post - operative pain control following orthopedic surgical procedures without excessive reliance upon opioid pain medication has garnered increased attention in recent years. This study will evaluate the utilization of a non-invasive, novel cryo - compression, post-operative modality to improve pain control versus standard ice wraps in the immediate post-operative phase of arthroscopic rotator cuff surgery via a randomized controlled study design. Furthermore, if this study demonstrates improved pain control, improved quality of life and decreased opioid usage with the intermittent cold compression unit, recommendations may be considered for system-wide utilization.
Eligibility criteria
Qualifiers
Patients who are candidates for arthroscopic rotator cuff repair
Acute, traumatic tear of the rotator cuff in an active patient
Chronic, symptomatic tear of the rotator cuff in an active patient having failed non - operative treatment
Patient agreeable to participation in the study and able to complete informed consent process and all study requirements.
Disqualifiers
Pregnancy (per pre-operative physical)
Presence of significant glenohumeral joint osteoarthritis
Age over 70
History of clinically diagnosed lymphedema
Trial design
Treatments tested in this trial
- Cryo-compression
- Cryo-therapy