Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06625723

Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery

Investigating the Impact of a Sleep Aid on Sleep and Recovery Following Rotator Cuff Repair Surgery

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
New York Presbyterian Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

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

Interventions

TypeNameDescription
PROCEDUREStandard postoperative careThis will include medications, rehabilitation schedules, and follow-up visits as normally scheduled.
DEVICESurgical Recovery Systems Sleep AidSleep assistive device

Timeline

Start date
2024-12-01
Primary completion
2026-10-01
Completion
2027-04-01
First posted
2024-10-03
Last updated
2024-11-18

Source: ClinicalTrials.gov record NCT06625723. Inclusion in this directory is not an endorsement.