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Efficacy and Safety of Intra-articular Injections of Frozen Platelet-Rich Plasma in Patients With Knee Osteoarthritis

This trial has no sites in United States.

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Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 85 years old?

Source: NCT07329361, who can take part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
MiKS Hospital
Trial code
NCT07329361
Record updated
9 January 2026
Original description
Evaluation of intra-articular injections in knee osteoarthritis using frozen-stored PRP. Compared with intra-articular injections of PRP applied at the time of collection.Read full original descriptionShow less

Efficacy and Safety of Intra-articular Injections of Frozen Platelet-Rich Plasma in Patients With Knee Osteoarthritis: Randomized Control Trial

Evaluation of intra-articular injections in knee osteoarthritis using frozen-stored PRP. Compared with intra-articular injections of PRP applied at the time of collection.

Inclusion: Patients of both sexes; Aged between 40 and 85 years old; Diagnosed with osteoarthritis through clinical radiological examination; Joint pain equal to or less than 75 points on the KOOS (pain); Radiological severity grades 1, 2, and 3 according to the Ahlbäck scale; Indication for intra-articular PRP infiltration; Body Mass Index values between 20 and 35; Negative serological tests for syphilis, HIV, HBV, and HCV; Possibility of observation during the follow-up period; Signature of informed consent.

Exclusion: Previous arthroscopy in the last year; Intra-articular corticosteroid or PRP injection in the last 6 months; Diagnosed polyarticular disease; Systemic autoimmune rheumatic disease (connective tissue diseases and systemic necrotizing vasculitis); Anemia or other hematological disorders; Positive serological tests for SYPHILIS, HIV, HBV, and HCV; Poorly controlled diabetes mellitus; Patients allergic to paracetamol; Body mass index >35; Severe mechanical deformity; Intra-articular hyaluronic acid injection in the last 12 months; Undergoing immunosuppressive treatments; Pregnancy or breastfeeding.

ClinicalTrials.gov NCT07329361