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Clinical Trials in Turkey / NCT07473232
Recruiting Not applicable

Comparison of Platelet-rich Plasma and Activated Cytokine-rich Serum Injection Treatments in Patients With Knee Osteoarthritis. (KOA PRP ACS)

NCT07473232 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-04-01
Last updated
2026-08-20

Condition(s) studied

Knee Arthritis OsteoarthritisPlatelet Rich Plasma InjectionConditioned Serum

Investigational drug(s) / intervention(s)

Autologous Platelet-Rich Plasma (PRP) →Conditioned serum (CS)

Autologous Platelet-Rich Plasma (PRP): Autologous Platelet-Rich Plasma (PRP) will be injected intra-articularly in patients with knee osteoarthritis

Conditioned serum (CS): Autologous conditionedserum (CS) will be injected intra-articularly in patients with knee osteoarthritis

Study summary

The effects of single dose injection of platelet rich plasma or conditioned serum in the knee joint in patients with knee osteoarthritis will be compared

Eligibility

Sex
ALL
Min age
40 Years
Max age
80 Years
Healthy volunteers
No
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) -

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Pamukkale University Hospital Pamukkale Denizli Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07473232 on ClinicalTrials.gov ↗ ← All trials in Turkey