Effects of Reparel™ Knee Sleeve on Knee Osteoarthritis

NACompletedINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

February 1, 2021

Primary Completion Date

November 6, 2021

Study Completion Date

November 6, 2021

Conditions
Knee Osteoarthritis
Interventions
DEVICE

Reparel Knee Sleeve

Patients who are recommended for non-operative management of knee osteoarthritis and have been consented in clinic to participate in the study will be given a Reparel™ knee sleeve to wear for knee osteoarthritis management. Each device will be numbered and recorded in the patient's REDCap entry for future reference if needed. Following administration of the Reparel™ knee sleeve, patients will be given instructions on how to use/wear the sleeve while performing activities of daily living or sports that had previously resulted in knee pain and also be asked to do the follows: wear the sleeve as much as they possibly can; not change their usual activities and diet during the time they are on this study; record in a diary the number of hours sleeve was worn per day; record any adverse effects or discomfort due to sleeve use; refrain from altering treatment for knee osteoarthritis.

Trial Locations (1)

35205

UAB Hospital Highlands, Birmingham

All Listed Sponsors
lead

University of Alabama at Birmingham

OTHER

NCT04743921 - Effects of Reparel™ Knee Sleeve on Knee Osteoarthritis | Biotech Hunter | Biotech Hunter