The Analysis of Efficacy Factors for Autologous Platelet-Rich Plasma Therapy in the Treatment of Elbow Tendinopathy

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age19+
SponsorCHA University

About this trial

To identify key factors influencing the effectiveness of platelet-rich plasma (PRP) therapy in treating elbow tendinopathy, a common degenerative condition.

Eligibility criteria

Qualifiers

Adults aged 19 years or older

Diagnosed with elbow tendinopathy

Persistent pain despite receiving conservative treatment

Disqualifiers

Individuals with systemic infection at the time of study participation

Patients with rheumatic diseases or inflammatory disorders

Individuals with unstable systemic conditions affecting the cardiovascular, gastrointestinal, respiratory, or endocrine systems

Any other cases deemed inappropriate for study participation by the investigator

Trial design

Treatments tested in this trial

  • Autologous Platelet-Rich Plasma (PRP) Injection

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators