Clinical Trial

Dry Needling vs ESWT in Lateral Epicondylitis

Active, Not Recruiting
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Summary
This randomized single-blind controlled trial aims to compare the effectiveness of ultrasound-guided dry needling and extracorporeal shock wave therapy in patients with lateral epicondylitis. Sixty participants aged 18-65 years will be randomized into two groups. The dry needling group will receive ultrasound-guided tendon fenestration once weekly for five sessions, while the ESWT group will receive radial extracorporeal shock wave therapy once weekly for five sessions. All participants will be given a standardized home exercise program. Pain, function, grip strength, pressure pain threshold, quality of life, and ultrasonographic findings will be evaluated at baseline, post-treatment, and at 3- and 6-month follow-up. The primary outcome is change in pain severity measured by Visual Analog Scale.
Protocol Amendment History 3 changes
critical Trial status changed: Not Yet Recruiting → Active, Not Recruiting 2026-08-07
notable Primary completion moved earlier: 2026-12-15 -> 2026-08-01 2026-08-07
minor Completion moved earlier: 2027-01-15 -> 2026-08-01 2026-08-07
Trial Details
NCT Number NCT07550322
Lead Sponsor Haydarpasa Numune Training and Research Hospital
Conditions Lateral Epicondylitis (Tennis Elbow)
Enrollment 60 participants
Start Date 2026-02-01
Primary Completion 2026-08-01 (estimated)
Study Completion 2026-08-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-06