Platelet-Rich Plasma (PRP) Injection for the Treatment of Chronic Patellar Tendinopathy

PHASE2CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

February 29, 2024

Study Completion Date

February 29, 2024

Conditions
Chronic Patellar TendinopathyChronic PT
Interventions
BIOLOGICAL

platelet rich plasma

A blood draw of 15 mL of the subject's own blood will be performed. The study coordinator will then place the sample in the Platelet Separator System (a centrifuge) and spin the blood sample in using a two-stage spinning: the 1st separates red blood cells from platelets, and the 2nd concentrates the platelets. This will be spun by centrifuge to yield 6 mL of concentrated autologous platelet. Under continuous ultrasound evaluation, 1.0-2.0 mL of the prepared PRP will be injected onto the origin of the patella tendon itself will be peppered along a short segment of the tendon into the areas of palpated tenderness and US-documented pathology.

OTHER

saline

A blood draw of 15 mL of the subject's own blood will be performed to maintain blinding. Under continuous ultrasound evaluation, 1.0-2.0 mL of the saline solution will be injected onto the origin of the patella tendon itself will be peppered along a short segment of the tendon into the areas of palpated tenderness and US-documented pathology.

Trial Locations (2)

53705

Wisconsin Institute of Medical Research, Madison

53711

UW Sports Medicine Clinic at Research Park, Madison

All Listed Sponsors
lead

University of Wisconsin, Madison

OTHER

NCT01843504 - Platelet-Rich Plasma (PRP) Injection for the Treatment of Chronic Patellar Tendinopathy | Biotech Hunter | Biotech Hunter