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Trials / Recruiting

RecruitingNCT05825105

Effectiveness of Platelet-rich Plasma Treatment of Knee Osteoarthritis

Efectividad Del Plasma Rico en Plaquetas (PRP) Para la disminución Objetiva Del Dolor y la recuperación Funcional Del Miembro Inferior en Osteoartritis de Rodilla. Evaluación de Alternativas metodológicas

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
110 (estimated)
Sponsor
Universidad Nacional de Entre Rios · Academic / Other
Sex
All
Age
35 Years
Healthy volunteers
Not accepted

Summary

Osteoarthritis (OA) is a disease that affects the joints of the body, causing pain, stiffness, and reduced mobility. To treat knee OA, a therapy called platelet-rich plasma (PRP) is used, which involves making a concentrated substance from the patient's own blood and injecting it into the joint. It has been shown that this therapy is effective in reducing pain; however, more research is needed to optimize the preparation and identify which patients are more receptive to the treatment. The primary objective of this study is to evaluate two modalities of PRP application and determine whether these treatments result in better pain reduction and improved functionality. The secondary objective is to explore the association between changes in LEFS questionnaire scores and/or maximal quadriceps isometric strength and possible clinical improvement.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPlatelet-Rich PlasmaThe PRP will be prepared using a single centrifugation process. Approximately 30 ml of peripheral blood will be drawn and collected into a vacutainer tubes with sodium citrate anticoagulant 0.129 mol/l (3.8%). The tubes will then be centrifuged at 900 RPM for 12 minutes at room temperature in a benchtop centrifuge. We will separate the lower third of the plasma fraction from all tubes with a syringe and needle, taking care to avoid the leukocyte layer. The PRP will be refrigerated at 4°C for no less than 1 hour. We will not use any exogenous factors to stimulate the platelet activation process. The periauricular skin surface will be disinfected with a povidone iodine solution, and an intra-articular local anesthetic with 1% lidocaine will be applied. A 21-gauge needle will be placed at the point of application. Finally, PRP will be injected into the joint, and the needle will be removed.

Timeline

Start date
2024-05-01
Primary completion
2025-09-01
Completion
2025-09-01
First posted
2023-04-24
Last updated
2024-05-20

Locations

1 site across 1 country: Argentina

Source: ClinicalTrials.gov record NCT05825105. Inclusion in this directory is not an endorsement.