Autologous Platelet-Rich Plasma (PRP)
DrugAutologous Platelet-Rich Plasma (PRP) will be injected intra-articularly in patients with knee osteoarthritis
NCT Number: NCT07473232
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
Trial opening soon.
Get Notified40 year–80 year
All sexes
Interventional
Not applicable
Patients with early grade bilateral knee osteoarthritis (Kellgren Lawrence grade 1 or 2) will be divided into 2 groups. One group of patients will be injected with single dose of autologous platelet rich plasma (PRP) in the knee joints. Other group of patients will be injected with eqiuvolume of autologous conditioned serum (CS) (also known as activated cytokine rich serum) in the knee joints. Patients' serum before injection, the treatment product (PRP and CS), patients serum 30 min after injection will be investigated for IL-1β, IL-1Ra, PDGF-BB, IGF-1, TGF-β and TNF-α. Patients' serum 1 week and 1 month after injection will be investigated for MMP-13, COMP by ELISA. Patients will also be investigated for visual pain scale, WOMAC (Western Ontorino and Mc Master) scale range of motion, ultrasonographic tibiofemoral cartilage thickness measurement and functional tests including the 30-second chair test, stair climb test, 40 meter fast paced walk test, timed up and go test, 6-minute walk test, and walking speed in the first week, first month and third month after injection.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Autologous Platelet-Rich Plasma (PRP) will be injected intra-articularly in patients with knee osteoarthritis
Autologous conditionedserum (CS) will be injected intra-articularly in patients with knee osteoarthritis
Time frame: Visual pain scale score (min 0-max 10) will be measured at the beginning ofthe study, 1 week, 1month and 3 months after the injection.
Visual pain scale score (min 0-max 10), higher scores indicate better results
Contact information is provided by the study sponsor or research team.
Pamukkale University
Other
Acronym: KOA PRP ACS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07236073
Arthritis, Joint Diseases
Erzurum, Turkey (Türkiye)
View Trial DetailsNCT06711445
Arthritis, Joint Diseases
Konya, Turkey (Türkiye)
View Trial DetailsNCT01412814
Arthritis, Joint Diseases
Haifa, Israel
View Trial DetailsNCT07666061
Knee Arthritis Osteoarthritis
View Trial Details