Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery

Sponsor
New York Presbyterian Hospital
Study ID
NCT06625723
Status
Not Yet Recruiting

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Conditions

  • Rotator Cuff Injuries
  • Rotator Cuff Tears
  • Shoulder Impingement
  • Shoulder Injuries
  • Shoulder Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Standard postoperative care — PROCEDURE
    This will include medications, rehabilitation schedules, and follow-up visits as normally scheduled.
  • Surgical Recovery Systems Sleep Aid — DEVICE
    Sleep assistive device

Study Details

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.

Key Dates

First listed
Oct 3, 2024
Start date
Dec 1, 2024
Status verified
Oct 2024
Primary completion
Oct 1, 2026
Completion
Apr 1, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Control Group
    Standard postoperative care for patients undergoing rotator cuff repair.
  • Experimental: Sleep Aid Group
    Standard postoperative care for patients undergoing rotator cuff repair PLUS the use of the sleep assistive device postoperatively.

Primary Outcome Measure

Narcotic Use [ Time Frame: Daily ]

Central Contacts

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