Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNew York Presbyterian Hospital
About this trial
Postoperative recovery following a rotator cuff repair surgery can be challenging. In particular, sleeping is difficult given the restrictions of the operative shoulder. This study aims to evaluate a postoperative sleep device that will allow for safe and comfortable positioning of the arm, with the anticipated effect to improve postoperative recovery and sleep.
Eligibility criteria
Qualifiers
Rotator Cuff Tear
Disqualifiers
Prior ipsilateral shoulder surgery
Ipsilateral upper extremity neurological deficit
Trial design
Treatments tested in this trial
- Standard postoperative care
- Surgical Recovery Systems Sleep Aid
Treatment groups
60 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov