Knee pain relief showdown: PRP vs. Cytokine-Rich serum
NCT ID NCT07473232
First seen Jun 27, 2026 · Last updated Aug 21, 2026 · Updated 2 times
Summary
This study will compare the effects of a single injection of platelet-rich plasma (PRP) versus conditioned serum (CS) in 60 people with knee osteoarthritis. Participants must have had knee pain for at least 6 months and meet specific criteria. The goal is to see which treatment better reduces pain, measured by a visual pain scale.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- platelet-rich plasma (PRP) and conditioned serum (CS)
- What this could lead to
- If successful, this could show which injection offers better pain relief for knee osteoarthritis, guiding future treatment choices.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, and results may not apply to all patients. Pain relief may be modest or temporary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Diagnosis of knee osteoarthritis according to ACR criteria at least 6 months ago. 2. Being between grade 1-2 according to the Kellgren-Lawrence radiological classification. 3. Not having had PRP injection in the last year. 4. Knee pain ≥ 5 according to the visual pain scale. Exclusion Criteria: 1. Those with significant neurological or cardiovascular disorders. 2. Those with active thrombovascular disease. 3. Those with joint or skin infections. 4. Those who have recently had an infectious disease. 5. Those infected with Hepatitis B, C, and HIV. 6. Those who have received intra-articular knee injections (hyaluronic acid, PRP, corticosteroids, and others) within the last year. 7. Those who use oral corticosteroids. 8. Those who have used NSAIDs within the last week. 9. Those who have used anti-platelet or anti-aggregant drugs within the last week. 10. Those with coagulation disorders. 11. Those with hemoglobin \<10 g/dl and platelet count \<100,000 12. Those with cancer. 13. Pregnant or breastfeeding women, drug addicts. 14. Those scheduled for knee surgery or arthroscopy, or those who have undergone knee surgery or arthroscopy. 15. Those with diseases causing secondary osteoarthritis: 1. post-traumatic, 2. congenital or developmental diseases 1. Local diseases (leg length discrepancy, varus, valgus deformities, hypermobility syndromes, scoliosis) 2. Generalized diseases (Bone dysplasias, Metabolic disorders (hemochromatosis, ochronosis, Gaucher disease, hemoglobinopathy, Ehlers-Danlos disease)) 3. Calcium storage diseases (calcium pyrophosphate storage disease, etc.) 4. Other bone and joint diseases (avascular necrosis, rheumatoid arthritis, gouty arthritis, septic arthritis, Paget's disease, osteoporosis, osteochondritis) 5. Other diseases 1. Endocrine diseases (Diabetes mellitus, acromegaly, hypothyroidism, hyperthyroidism) 2. Neuropathic arthropathy (Charcot joint) 3. Other (Frost, Kashin-Beck disease, Caisson disease) -
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Pamukkale University Hospital
RECRUITINGPamukkale, Denizli, 20070, Turkey (Türkiye)
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