Utility of Intermittent Cryo-Compression Versus Traditional Icing Following Arthroscopic Rotator Cuff Repair

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorAllina Health System

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

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators