By InvitationNot Applicable

Clinical Outcomes Related to Arthroscopic Rotator Cuff Repair Recovery Using Incrediwear

United States140 participantsStarted 2024-11-11

Plain-language summary

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.

Who can participate

Age range18 Years – 75 Years

SexALL

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Inclusion criteria

✓. 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.

Exclusion criteria

✕. 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

What they're measuring

Arm Circumference Measure with a Measuring tape

Timeframe: Preop appointment, Postop Day 42, Day 84, Day 168, Day 364

Trial details

NCT IDNCT06669741

SponsorTexas Bone and Joint

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12-01

View on ClinicalTrials.gov More Rotator Cuff Tears trials