Clinical Trial

Clinical Trial to Evaluate the Efficacy and Safety of Platelet-rich Plasma Infiltration in Chronic Omalgia

Recruiting Phase 3
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Summary
The experimental group will receive intralesional injections of platelet-rich plasma, evaluating its ability to relieve pain and provide sustained improvement through biological modulation of the joint and tendon environment. In contrast, the control group will be treated with a combination of betamethasone and ropivacaine, representing the current standard of care for short-term inflammatory pain management. The comparison between these two options will determine whether platelet-rich plasma offers advantages in terms of clinical efficacy and duration of benefits. The results obtained could contribute significantly to the development of more effective protocols and more precise management guidelines for patients with chronic omalgia, thus addressing existing controversies and improving clinical practice.
Trial Details
NCT Number NCT07448285
Lead Sponsor Biobizkaia Health Research Institute
Conditions Chronic Pain
Enrollment 86 participants
Start Date 2026-02-24
Primary Completion 2029-02 (estimated)
Study Completion 2029-04 (estimated)
Updated on ClinicalTrials.gov 2026-03-04