Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
COMPLETED
NCT07042997
NA

Anatomical Accuracy of Palpation-Guided Dry Needling in Lateral Epicondylitis

Sponsor: nurmuhammet tas

View on ClinicalTrials.gov

Summary

This prospective study evaluated the anatomical accuracy of palpation-guided dry needling in patients with lateral epicondylitis using ultrasound verification. The study included 39 participants aged 18-70 years with lateral elbow pain lasting at least six weeks and at least one active myofascial trigger point in the forearm extensor muscles. The target muscle was selected based on the lowest pressure pain threshold among the evaluated muscles. Dry needling was performed using anatomical landmarks and palpation without real-time ultrasound guidance. Immediately after needle placement, an independent ultrasound assessor, blinded to the intended target muscle, identified the actual location of the needle tip. The primary outcome was the proportion of correctly placed needles in the intended target muscle. Accuracy was evaluated separately for the brachioradialis, extensor carpi radialis brevis, extensor carpi radialis longus, and extensor digitorum communis muscles.

Official title: Anatomical Accuracy of Palpation-Guided Dry Needling in Lateral Epicondylitis: An Ultrasound-Verified Study of Forearm Extensor Muscles

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

39

Start Date

2025-06-24

Completion Date

2025-07-30

Last Updated

2026-10-26

Healthy Volunteers

No

Interventions

PROCEDURE

Palpation-Guided Dry Needling With Ultrasound Verification

A single experienced physician performed palpation-guided dry needling of one selected forearm muscle (EDC, ECRB, ECRL, or BR) using a sterile Hua-Long 0.30 × 30 mm acupuncture needle. The target muscle was selected according to the lowest pressure pain threshold. Ultrasound was used to confirm algometer positioning before needling but was not used to guide needle insertion. Following a minimum 10-minute interval after algometric assessment, dry needling was performed using anatomical landmarks and palpation. Immediately after needle insertion, an independent sonographer, unaware of the intended target muscle, identified the needle-tip location using a 5-12 MHz linear ultrasound probe. Placement was classified as correct or incorrect according to whether the needle tip was located within the intended target muscle.

Locations (1)

Basaksehir Cam and Sakura City Hospital

Istanbul, Istanbul, Turkey (Türkiye)