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NOT YET RECRUITING
NCT07042997
NA

Ultrasound Evaluation of Blind Dry Needling in Lateral Epicondylitis

Sponsor: nurmuhammet tas

View on ClinicalTrials.gov

Summary

The aim of this clinical study is to evaluate the accuracy and consistency of the blinded needling procedure by evaluating the dry needling procedure under ultrasound guidance in patients diagnosed with lateral epicondylitis and with at least one active trigger point (MTrP) in the forearm extensor muscles. The study is a prospective, double-blind validation study. Participants: Volunteers aged 18-70 years, who have pain in the lateral epicondyle region for at least 6 weeks and who have active trigger points in the forearm extensor muscles detected by physical examination will be included in the study. Written informed consent will be obtained from all participants.

Official title: Evaluation of Anatomical Accuracy in Targeting Forearm Extensor Muscles With Blind Dry Needling in Patients With Lateral Epicondylitis Using Ultrasound Guidance

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-09-21

Completion Date

2025-09-23

Last Updated

2025-09-15

Healthy Volunteers

No

Interventions

PROCEDURE

Evaluation of Anatomical Accuracy in Targeting Forearm Extensor Muscles with Blind Dry Needling in Patients with Lateral Epicondylitis Using Ultrasound Guidance

Using a high-resolution linear probe (5-12 MHz) , the muscle in which the needle tip is located is monitored in real time in the transverse and longitudinal planes. Whether the needle is in the targeted muscle is recorded as "correct" or "incorrect".