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COMPLETED
NCT07550322
NA

Dry Needling vs ESWT in Lateral Epicondylitis

Sponsor: Haydarpasa Numune Training and Research Hospital

View on ClinicalTrials.gov

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.

Official title: Ultrasound-Guided Dry Needling Versus Extracorporeal Shock Wave Therapy in Lateral Epicondylitis: A Randomized Single-Blind Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-02-01

Completion Date

2026-09-14

Last Updated

2026-09-16

Healthy Volunteers

No

Interventions

PROCEDURE

Ultrasound-guided dry needling

Dry needling will be performed under ultrasound guidance targeting the tendinosis area of the common extensor tendon. The procedure will be applied once weekly for five sessions.

DEVICE

Extracorporeal Shock Wave Therapy

Radial extracorporeal shock wave therapy will be applied using standard parameters (10-15 Hz, 1.5-2.5 bar, 2000 pulses) once weekly for five sessions.

Locations (1)

Haydarpasa Numune Training and Research Hospital

Istanbul, Istanbul, Turkey (Türkiye)