Conventional Platelet-Rich Plasma Versus Concentrated Bone Marrow Stem Cell Injections for Osteoarthritis of the Knee

Mayo Clinic

Status and phase

Withdrawn

Phase 2

Conditions

Osteo Arthritis Knee

Treatments

Biological: Platelet-Rich Plasma (PRP)

Biological: Concentrated Bone Marrow Aspirate (BMAC)

Study type

Interventional

Funder types

Other

Identifiers

NCT03271229

15-008718

Details and patient eligibility

About

Previous clinical trials have demonstrated the human body's own healing and regenerative cells can relieve the pain of arthritis. Bone marrow contains stem cells which can change into cells of various different tissue types, while platelet rich plasma contains growth factors. Both techniques have been shown to relieve pain and with this study the Investigators wish to compare the two treatments.

Full description

Participants will be randomized into two groups. Concentrated Bone Marrow Aspirate (BMAC) or Platelet-Rich Plasma (PRP). BMAC subjects will have bone marrow aspirated from the subjects iliac crests and the cellular rich portion will be concentrated and subsequently injected into the subjects' symptomatic knee. BMAC patients will also have a venous whole blood drawn from the antecubital vein to simulate a PRP procedure. PRP subjects will have the same venous blood draw from the antecubital vein with subsequent platelet concentration. The resulting PRP will be injected into the symptomatic knee. PRP subjects will also undergo a bone marrow aspiration from the iliac crest to simulate the BMAC procedure. Follow-up at 1 week, 6 weeks, 6 months, and 12 months after injection, with repeat radiographs at 12 months.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects must have bilateral OA and pain in one knee.
Osteoarthritis may be primary or secondary. Knees must have Kellgren-Lawrence Grades 1-3.
Subjects must have previously tried 6 weeks of one of the following conservative treatments: Activity modification, weight loss, physical therapy, anti-inflammatory, or injection therapy.
Patients must be able to provide written informed consent after the nature of the study is fully explained.

Exclusion criteria

Patients with abnormal hematology, serum chemistry, or screening laboratory results.
Patients taking anti-inflammatory medications (prescription or over-the-counter), including herbal therapies, within 14 days of baseline visit.
Patients taking anti-rheumatic disease medication (including methotrexate or other antimetabolites) within the 3 months prior to study entry.
Patients receiving injections to the treated knee within 3 months prior to study entry.
Patients who are pregnant or currently breast-feeding.
Patients with systemic, rheumatic, or inflammatory disease of the knee or chondrocalcinosis, hemochromatosis, inflammatory arthritis, arthropathy of the knee associated with juxta-articular Paget's disease of the femur or tibia, ochronosis, hemophilic arthropathy, infectious arthritis, Charcot's knee joint, villonodular synovitis, and synovial chondromatosis.
Patients with ongoing known infectious disease.
Patients with clinically significant cardiovascular, renal, hepatic, endocrine disease, or cancer.
Patients participating in a study of an experimental drug or medical device within 30 days of study entry.