Platelet-rich plasma injections in and around the knee for knee osteoarthritis
Compares platelet-rich plasma injected inside and around the knee versus inside only, in knee osteoarthritis.
Key facts
- Who runs it
- Ankara City Hospital Bilkent
- Where
- Türkiye1 site in 1 countryChoose a country to see its sites
- Trial code
- Registry title
- The Effects of Intra-articular and Peri-articular Platelet-rich Plasma (PRP) Injections ın Chronic Knee Osteoarthritis
- Status
- Recruiting
- People taking part
- 42 people, planned
- Started
- 1 Aug 2025
- Planned end
- 30 Apr 2026
- Type of study
- Interventional, 3 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- Conservative Therapy
- Intra-Articular PRP
- Peri-Articular PRP
- Record updated
- 15 January 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with long-lasting knee osteoarthritis (wear of the knee joint) and pain on the inner side of the knee. It compares exercise advice alone with added PRP injections (from your own blood) into and around the knee.
- Age
- 40 to 65 years
- Sex
- All sexes can join.
- Disease stage
- Knee osteoarthritis by the American College of Rheumatology (ACR) criteria, Kellgren-Lawrence grade 2 or 3 on X-ray. Pain score (VAS) of 4 or higher.
- Earlier treatment
- Medial knee pain not helped by conservative treatment for at least 3 months. No physical therapy, steroid or hyaluronic acid injections in the knee in the last 3 months. No NSAIDs in the last week.
Main reasons for not taking part
- Past knee injury or knee surgery
- Active cancer, infection, hepatitis or a weak immune system
- Bleeding problems, irregular INR from warfarin, or anemia
- Inflammatory joint disease, or use of corticosteroids or opioids
- Pregnancy (suspected or confirmed) or body mass index (BMI) greater than 35
The registry criteria, word for word
Show all 23 criteriaShow less
Who can take part
- Age between 40 and 65 years
- Patients with significant medial knee pain who have not responded to conservative treatment for at least 3 months
- Patients diagnosed with knee osteoarthritis according to the American College of Rheumatology (ACR) criteria and with Kellgren-Lawrence grade 2 or 3 radiographic osteoarthritis
- Intact cognitive function
- Willingness to participate in the study and provide signed informed consent
- Visual Analog Scale (VAS) score of 4 or higher
Who cannot take part
- History of previous knee trauma or surgery
- Physical therapy, intra-articular steroid, or hyaluronic acid injections in the knee within the last 3 months
- Use of corticosteroids or opioids
- Active oncological diseases
- Local infection, sepsis, wounds, or scars in the injection area
- Systemic infections, hepatitis, or immunosuppression
- Uncontrolled hypertension, uncontrolled diabetes mellitus, decompensated heart failure, coronary artery disease, or asthma
- Allergy to citrate
- General health impairment or lack of cooperation
- Bleeding diathesis or irregular International Normalized Ratio (INR) due to oral warfarin use
- Use of nonsteroidal anti-inflammatory drugs (NSAIDs) within the last week that may affect platelet function analyzer-100 (PFA-100) activity
- Inflammatory arthropathies
- Suspected or confirmed pregnancy
- Anemia
- Body mass index (BMI) greater than 35
- Physical examination findings suggestive of patellar retinaculum, meniscus, or cruciate ligament injury
- Refusal to participate in the study
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 40 and 65 years old?
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
The primary objective of this study is to evaluate and compare the effectiveness of ultrasound-guided combined intra-articular and peri-articular platelet-rich plasma (PRP) injections with intra-articular PRP injections alone in patients with chronic knee osteoarthritis (OA). The study specifically examines the effects of these treatment approaches on pain, physical function, activities of daily living, and structural parameters, including medial collateral ligament (MCL) thickness and distal femoral cartilage thickness.
Read full original descriptionShow less
Osteoarthritis is a degenerative joint disease characterized by progressive cartilage erosion, osteophyte formation, and subchondral sclerosis, leading to pain, stiffness, and functional disability. It is the most common form of arthritis and a leading cause of disability worldwide, affecting approximately 300 million individuals. Although the knee is the most frequently involved joint, OA is now recognized as a whole-joint disease, involving not only cartilage degeneration but also pathological changes in subchondral bone, synovium, and surrounding extra-articular structures.
Platelet-rich plasma is an autologous concentration of platelets suspended in a small volume of plasma and contains a variety of bioactive growth factors, such as transforming growth factor-beta (TGF-β), platelet-derived growth factor (PDGF), and vascular endothelial growth factor (VEGF). These factors play a crucial role in promoting cell proliferation, angiogenesis, and tissue repair. In knee OA, PRP has been shown to reduce matrix metalloproteinase (MMP) activity, particularly MMP-13, enhance endogenous hyaluronic acid production, and support chondrogenesis. Although intra-articular PRP injections are widely accepted as a safe and effective treatment and have demonstrated superiority over placebo and hyaluronic acid in long-term follow-up studies, most existing research has focused exclusively on intra-articular applications.
Knee OA is a multifactorial condition frequently associated with extra-articular pathologies, including ligament laxity, peri-articular edema, and soft tissue inflammation. Limiting treatment to the intra-articular space alone may therefore overlook these important contributors to pain and functional impairment. Emerging evidence suggests that a combined treatment approach targeting both intra-articular and peri-articular structures may provide superior outcomes in terms of pain reduction and functional improvement.
This prospective randomized controlled trial will include 42 patients aged 40-65 years with chronic knee OA classified as Kellgren-Lawrence grade 2 or 3. Participants will be randomly assigned to one of three groups: a control group receiving conservative treatment only (exercise therapy and lifestyle modifications), a group receiving conservative treatment plus ultrasound-guided intra-articular PRP injections, and a third group receiving conservative treatment plus combined ultrasound-guided intra-articular and peri-articular PRP injections targeting the MCL and pes anserinus regions.
Clinical outcomes will be assessed using validated instruments, including the Visual Analog Scale (VAS), the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and the Short Form-36 (SF-36) Quality of Life Scale. In addition, ultrasonographic measurements of MCL thickness and distal femoral cartilage thickness will be performed to evaluate structural changes. By investigating the additional value of peri-articular PRP injections, this study aims to contribute to the development of more comprehensive and effective injection protocols for the management of chronic knee osteoarthritis.
The 3 groups in the trial
- Control GroupExisting treatment, for comparison
Patients receiving guidance on conservative exercise therapy and lifestyle chang
Treatment: Conservative Therapy
- Intra-articular PRPExisting treatment, for comparison
Patients receiving intra-articular PRP therapy in addition to guidance on conservative exercise therapy and lifestyle chang
Treatment: Conservative Therapy and Intra-Articular PRP
- Combinated PRP (Intra and peri-articular PRP)Existing treatment, for comparison
Patients receiving combined (periarticular and intraarticular PRP therapy) in addition to guidance on conservative exercise therapy and lifestyle chang
Treatment: Conservative Therapy, Intra-Articular PRP, and Peri-Articular PRP
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- The Effects of Platelet-rich Plasma (PRP) Injections Administered Into Intra-articular and Periarticular Regions Under Ultrasound Guidance in Chronic Knee Osteoarthritis on Pain, Function, Activities of Daily Living, Medial Collateral Ligament (MCL) and Distal Femoral Cartilage Thickness
- Plain-language title
- Platelet-rich plasma injections in and around the knee for knee osteoarthritisGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 14 November 2026.
- Fit questions
- Built from NCT07339137, who can take part
- Record updated
- 15 January 2026