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NCT06625723

Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery

Not yet recruiting NA Last updated 18 November 2024
What this trial tests

NA trial testing Standard postoperative care in Rotator Cuff Tears in 60 participants. Not yet recruiting.

Timeline
1 December 2024
Primary endpoint
1 October 2026
1 April 2027

Quick facts

Lead sponsorNew York Presbyterian Hospital
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date1 December 2024
Primary completion1 October 2026
Estimated completion1 April 2027

Drugs / interventions tested

Conditions studied

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:

Other trials of Standard postoperative care

Trials testing the same drug.

Other recruiting trials for Rotator Cuff Tears

Currently open trials in the same condition.

Other New York Presbyterian Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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