Clinical Research Directory

Inclusion Criteria: * • Scheduled to undergo primary unilateral anterior cruciate ligament reconstruction with either bone patella tendon bone, quadriceps tendon or Achillies allograft. * Subject is willing and able to comply with study instructions and commit to all follow-up visits for the duration of the study Exclusion Criteria: * • Any records flagged "break the glass" or "research opt out" * Prior ligamentous injury and/or surgery to the operative knee (arthroscopic surgeries allowed), previous ACL surgery of the target knee, previous graft failure, or relevant musculoskeletal impairment * Any pain disorder, neuro-muscular disorder, or neuropathy * History of opioid or alcohol abuse within past 3 years * Open and/or infected wound in the treatment areas or any local skin condition at the treatment sites that in the Investigator's opinion would adversely affect treatment or outcomes * History of sensitive skin * History of known to be allergic to acrylic acid * History of implanted electronic devices (for example a cardiac pacemaker) * History of recently diagnosed or suspected DVT * History of cryoglobulinemia * History of paroxysmal cold hemoglobinuria * History of cold urticaria * History of Raynaud's disease * Concomitant surgical interventions * Recent incision on lateral leg