Effect of dry needling on dorsal myofascial pain syndrome

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effectiveness of dry needling treatment in patients diagnosed with Dorsal Myofascial Pain Syndrome. It involves a double-blind, sham-controlled, randomized trial with 60 participants aged 18 to 80 years who will receive either real or sham dry needling under ultrasound guidance. Both groups will be instructed on specific exercises to perform during the study period. The aim is to assess the impact of dry needling on pain relief and muscle sensitivity in the affected areas.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Clinically diagnosed with Dorsal Myofascial Pain Syndrome associated with rhomboid and trapezius trigger point.
* Having a shoulder pain Visual Analog Scale (VAS) score of 6 or higher.
* Ability to read and write

Exclusion Criteria:

* History of spinal surgery.
* Lesions, atrophy, or scars in the skin around the back.
* Undergoing physiotherapy targeting the back and lumbar region in the last 6 months.
* Undergoing an interventional procedure for back or lumbar pain in the last 3 months.
* Use of steroids in the last 1 month.
* Special conditions such as epilepsy, pregnancy, injection phobia, etc.
* Inability to comply with the restriction on the use of steroid and non-steroidal anti-inflammatory drugs during the treatment period.

Where it's running

• Kütahya Health Sciences University
  Kütahya, Turkey (Türkiye) Recruiting

Study contacts

• Principal investigator: Hasan H Gökpınar, Ass. Prof. — Kutahya Health Sciences University
• Study coordinator: Hasan H Gökpınar, Ass. Prof.
• Email: hasanhuseyin.gokpinar@ksbu.edu.tr
• Phone: 05052842222

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.