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Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery

NCT06625723 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-11-18

No results posted yet for this study

Summary

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.

Conditions

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

Interventions

PROCEDURE

Standard postoperative care

This will include medications, rehabilitation schedules, and follow-up visits as normally scheduled.

DEVICE

Surgical Recovery Systems Sleep Aid

Sleep assistive device

Sponsors & Collaborators

  • New York Presbyterian Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-01
Primary Completion
2026-10-01
Completion
2027-04-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06625723 on ClinicalTrials.gov