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Platelet Rich Plasma for Musculoskeletal Conditions (PRP for MSK)

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Not yet enrolling

Conditions

Elbow Osteoarthritis
Epicondylitis of the Elbow
Osteoarthritis (OA)
Plantar Fasciitis of Both Feet
Osteoarthritis (OA) of the Shoulder
Osteoarthritis (OA) of the Knee
Tendinopathy
Osteoarthritis Ankle
Osteoarthritis (OA) of the Hip

Treatments

Biological: Platelet Rich Plasma Injection
Device: Platelet Rich Plasma Preparation

Study type

Interventional

Funder types

Other

Identifiers

NCT07231471
00191115

Details and patient eligibility

About

The primary purpose of this study is to follow patients with various musculoskeletal (MSK) conditions over a one-year follow-up period after receiving a platelet rich plasma (PRP) injection, assessing changes in their pain levels, functional abilities, and overall patient satisfaction.

This will develop a robust registry of patients treated with PRP for a range of MSK conditions. These conditions include, but are not limited to, osteoarthritis (OA) of the knee, hip, glenohumeral joint, elbow, ankle, and sacroiliac joint, as well as rotator cuff tendinopathy, lateral and medial epicondylitis, plantar fasciitis, patellar tendinopathy, Achilles tendinopathy, and proximal hamstring tendinopathy.

Full description

Platelet-Rich Plasma (PRP) is an injectable preparation of a patient's blood that can be used for numerous conditions and has received significant attention over the past several years for its potential application for the treatment of pain and functional impairment due to osteoarthritis (OA) and other musculoskeletal conditions. Research on PRP has expanded dramatically over the last several decades, elevating its status from snake oil to a proven injection option superior to corticosteroids. It has demonstrated superior efficacy to standard-of-care corticosteroids in numerous musculoskeletal conditions. Systematic reviews of randomized-controlled trials have demonstrated equivalent-to-superior treatment outcomes associated with the use of intra-articular PRP compared to placebo, hyaluronic acid, and corticosteroid for the most commonly-studied condition, knee OA. Most importantly, just as corticosteroids have been used in numerous musculoskeletal conditions (OA, tendinopathy, bursitis, etc.), PRP has the same potential, but with vastly reduced risk; corticosteroids have many known dangers. To summarize, PRP has demonstrated level 1 evidence of superiority to corticosteroids in pain and function in numerous musculoskeletal conditions, with considerably less risk.

This study will evaluate pain, function, and overall patient satisfaction outcomes for the use of PRP for the treatment of a diverse MSK conditions, including, but not limited to, OA of the knee, hip, glenohumeral joint, elbow, ankle, and sacroiliac joint, as well as rotator cuff tendinopathy, lateral and medial epicondylitis, plantar fasciitis, patellar tendinopathy, Achilles tendinopathy, and proximal hamstring tendinopathy.

Enrollment

10,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18+ years old
  • Musculoskeletal pathology that may benefit from a PRP injection
  • Failed other conservative treatments

Exclusion criteria

  • No active malignancy
  • No active infection in the area of injection
  • No platelet disorder
  • No active systemic infections
  • No patients currently undergoing dialysis

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10,000 participants in 1 patient group

Platelet Rich Plasma Injection
Experimental group
Description:
Participants who are eligible and provide consent to participate will undergo a Platelet-Rich Plasma (PRP) injection. Their whole blood and the produced PRP will be analyzed using a cell counter, and they will be asked to complete follow-up surveys at 2 weeks, 6 weeks, 3 months, 6 months, and 12 months..
Treatment:
Device: Platelet Rich Plasma Preparation
Biological: Platelet Rich Plasma Injection

Trial contacts and locations

1

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Central trial contact

Luke A Johnson, BS; Jamie Egbert, MS

Data sourced from clinicaltrials.gov

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