Clinical Trial

Evaluation of Platelet-Rich Plasma (PRP) Treatment in Tendinopathies

Study acronym: RWE-TDP-PRP
Recruiting
View on ClinicalTrials.gov →
Summary
This multicenter, prospective, observational study, based on real-world evidence (RWE), aims to evaluate the efficacy and safety of Platelet-Rich Plasma (PRP) treatment across four types of tendinopathies: patellar, Achilles, epicondylar, and plantar fasciosis. Data collection and analysis will be conducted using the BioSmartData® platform, including hematology analyzers for PRP characterization, clinical variables, treatment protocols, and longitudinal assessment of therapeutic response.
Trial Details
NCT Number NCT07558564
Lead Sponsor ReSport Clinic
Collaborators: BioSmartData
Conditions Patellar Tendinopathy, Achilles Tendinopathy (AT), Epicondylitis, Lateral, Plantar Fasciitis, Chronic
Enrollment 2,000 participants
Start Date 2026-04
Primary Completion 2028-03 (estimated)
Study Completion 2028-03 (estimated)
Updated on ClinicalTrials.gov 2026-04-30