NCT06669741

Clinical Outcomes Related to Arthroscopic Rotator Cuff Repair Recovery Using Incrediwear

Enrolling by Invitation
NAAges 18–75InterventionalTreatment
Texas Bone and Joint
~140 participants
Updated 2025-05-08 on ClinicalTrials.gov
What's tested:PlaceboShoulder Sleeve

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Arm Circumference Measure with a Measuring tape
Measured over Preop appointment, Postop Day 42, Day 84, Day 168, Day 364
Rotator Cuff Tears
Rotator Cuff Injuries
Rotator Cuff Arthropathy of Left Shoulder (Disorder)
Rotator Cuff Arthropathy of Right Shoulder (Disorder)
Rotator Cuff Arthropathy of Bilateral Shoulders

NCT06669741

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Medical City Denton

    Denton, Texasno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Christopher L. Flowers · PRINCIPAL_INVESTIGATOR · Texas Bone and Joint

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Arm Circumference Measure with a Measuring tapePreop appointment, Postop Day 42, Day 84, Day 168, Day 364

    To measure swelling in the upper arm, a soft tape measure to measure the circumference of the arm at multiple points at the writs, mid-forearm, axilla, and oblique. A 2cm difference between arms at each area of the wrist, mid-forearm, axilla, and oblique shoulder is not optimal. Less than 2cm difference between arms at each area of the wrist, mid-forearm, axilla, and oblique shoulder is optimal.