Last reviewed · How we verify
NCT06625723
Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery
NA trial testing Standard postoperative care in Rotator Cuff Tears in 60 participants. Not yet recruiting.
1 October 2026
Quick facts
| Lead sponsor | New York Presbyterian Hospital |
|---|---|
| Phase | NA |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 December 2024 |
| Primary completion | 1 October 2026 |
| Estimated completion | 1 April 2027 |
Drugs / interventions tested
- Standard postoperative care
- Surgical Recovery Systems Sleep Aid
Conditions studied
- Rotator Cuff Tears — all drugs for Rotator Cuff Tears →
- Rotator Cuff Injuries — all drugs for Rotator Cuff Injuries →
- Shoulder Pain — all drugs for Shoulder Pain →
- Shoulder Injuries — all drugs for Shoulder Injuries →
Sponsor
New York Presbyterian Hospital
Who can join
18 and older, any sex, with Rotator Cuff Tears or Rotator Cuff Injuries. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own 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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06625723
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Standard postoperative care
Trials testing the same drug.
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Other recruiting trials for Rotator Cuff Tears
Currently open trials in the same condition.
- NCT07383038 — Effect of Mobilization With Movement in Patients With Rotator Cuff Lesions · NA · recruiting
- NCT06918041 — FiberLocker® System Augmentation of Rotator Cuff Repairs · NA · recruiting
- NCT06886932 — Pain Education After Rotator Cuff Surgery · recruiting
- NCT07001566 — The Impact of Cervical Radiculopathy on Functionality in Patients Undergoing Rotator Cuff Repair · recruiting
- NCT06733480 — Innovating Physical Therapy: A Pilot Study on Band Connect's Impact on Compliance, Satisfaction, and Revenue · NA · recruiting
Other New York Presbyterian Hospital trials
Trials by the same sponsor.
- NCT05764382 — Remote Tai Ji for Low Back Pain · NA · unknown
- NCT05146583 — Injection of Autologous Bone Marrow Aspirate in Patients With Degenerative Disc Disease. · unknown
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- NCT03388320 — Using Addiction Comprehensive Health Enhancement Support System (ACHESS) in an Alcoholic Liver Disease Population · NA · unknown
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06625723 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by New York Presbyterian Hospital
- Last refreshed: 18 November 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06625723.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing