Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
study ends around
Principal Investigator
by Anthony Luke, MD (ucsf)
Headshot of Anthony Luke
Anthony Luke

Description

Summary

The investigators would like to study the differences in the quality of Platelet Rich Plasma (PRP) between two different machines in those with knee osteoarthritis. Knee osteoarthritis means your cartilage has been worn down, and it affects your knee joint. Both machines, the APEX Biologix XCELL PRP System and the Emcyte PurePRP Supraphysiologic Concentrating System, are FDA approved, commercially available, and makes PRP. The investigators will check if the platelets in the PRP have different amounts or work differently. The investigators will also assess participants symptoms after the injection and compare the two different preparation systems.

Keywords

Knee Osteoarthristis, Cartilage Damage, Platelet Rich Plasma, Platelet Rich Plasma Injection, Emcyte PurePRP Supraphysiologic Concentrating System, APEX Biologix XCELL PRP System

Eligibility

You can join if…

Open to people ages 18 years and up

  • Kellgren-Lawrence (KL) Grade 1-3 knee osteoarthritis
  • Symptoms of knee osteoarthritis for at least 3 months before presentation in one knee
  • Will be able to attend and perform physical therapy

You CAN'T join if...

  • Received injection therapy for knee osteoarthritis in the past 6 months
  • Have severe arthritis diagnosed in ≥1 major joint by radiology criteria
  • History of septic arthritis
  • Underwent knee surgery for osteoarthritis or osteochondral defects within 1 year before randomization (e.g., autograft or allograft surgery)
  • Have had high tibial osteotomy, partial knee replacement, patellar resurfacing, total knee replacement, or have existing surgical hardware in the knee
  • Received a platelet-rich plasma injection elsewhere in the body within the past 3 months
  • Have a platelet disorder or bleeding disorder
  • Have a rheumatologic disease, autoimmune disorder, immunocompromised status, or active history of cancer
  • Are taking chemotherapy, require regular prednisone, or require regular anti-inflammatory use
  • Are pregnant, breastfeeding, or unwilling to practice birth control during the study
  • If both knees have osteoarthritis and the other knee has KL score equal to or greater than 2.
  • Have uncontrolled illness, physical disability, or other contraindication to aerobic exercise training

Location

  • University of California San Francisco
    San Francisco California 94158 United States

Lead Scientist at University of California Health

  • Anthony Luke, MD (ucsf)
    My clinic is busy and allows access to patients of any age, different activity levels, and various orthopedic and medical conditions. My experience enables me to manage patient issues conservatively while directing operative cases to our surgeons, improving the efficiency of the sports medicine service and surgical yield for surgeons.

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT07491367
Phase
Phase 4 research study
Study Type
Interventional
Participants
Expecting 20 study participants
Last Updated