Clinical Outcomes Related to Arthroscopic Rotator Cuff Repair Recovery Using Incrediwear

Enrolling by invitation · Not applicable · Has a placebo group

Conditions studied: 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

In brief

To assess the benefits of using the Incrediwear products for patients recovering from Arthroscopic Rotator Cuff Repair surgery for postoperative pain, range of motion, and swelling.

Key facts

Study ID

NCT06669741

Run by

Texas Bone and Joint

People needed

140

Starts

2024-11-11

Expected to finish

2026-12-02

Last updated by the study team

2025-05-08

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients undergoing arthroscopic rotator cuff repair
• Patients aged 18-75
• Patients who are willing and able to adhere to follow-up schedule and protocol guidelines.
• Patients who are willing and able to sign corresponding research subject consent form.

You may not qualify if…

• Patient has a history of neurological conditions, including multiple sclerosis or Parkinson's disease
• Patient has severe medical condition, including recent myocardial infarction, unstable angina, heart failure, severe anemia
• Patient has had prior surgical treatment of a shoulder injury in the past 5 years
• Patient has chronic pain conditions unrelated to shoulder condition
• Patient has auto-immune or auto-inflammatory diseases
• Patient has used tobacco within the last 90 days
• Patient is not within the ages of 18-75
• Patient has poorly controlled diabetes with HgA1c > 7.5
• Patient has an active infection (local or systemic)
• Patient is unwilling or unable to sign the corresponding research subject consent form
• Patient meets any other criteria or has any other condition that, in the opinion of the investigator, would prevent them from completing the study or that, in the opinion of the investigator, would confound study results.
• Against medical advice (AMA)
• Prisoner as indicated in the medical record

Where it is running

• Medical City Denton — Denton, Texas, United States

Full record on ClinicalTrials.gov

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