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The Effectiveness of Dry Needling Treatment in Patients With Shoulder Myofascial Pain Syndrome

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 12 months later Nov 15, 2025 → Nov 15, 2026
See other at-risk trials from Kutahya Health Sciences University

Record History

  1. Notable Primary completion pushed from Nov 15, 2025 to Nov 15, 2026
    • Study completion pushed from Dec 15, 2025 to Dec 15, 2026
    v4
  2. Notable Primary completion date: Apr 15, 2025 to Nov 15, 2025
    • Study completion date: May 15, 2025 to Dec 15, 2025
    v3
  3. Notable Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Primary completion date: Jun 25, 2024 to Apr 15, 2025
    • Study sites: 0 to 1
    • Study completion date: Jun 25, 2024 to May 15, 2025
    • Start date changed from estimate of Mar 25, 2024 to Apr 25, 2024
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Myofascial pain can be diagnosed by the presence of one or more myofascial trigger points (MTrPs), defined as hyperirritable spots in taut bands of skeletal muscle fibers palpable by hand. The treatment of myofascial pain primarily relies on the inactivation of MTrPs, often through manual pressure techniques or dry needling. In manual pressure techniques, the physiotherapist applies increasing pressure directly to the MTrP. In dry needling, acupuncture-like filiform needles are applied to the same point. There are two types of dry needling: superficial dry needling, which penetrates only the skin and superficial muscle, and deep dry needling, which involves inserting a needle directly into the MTrP. The sole or adjunct effectiveness of dry needling treatment targeting the trapezius and infraspinatus muscles has been investigated, particularly in patients with shoulder myofascial pain syndrome. In the study we are planning, a double-blinded efficacy trial will be conducted in patients with shoulder myofascial pain syndrome, where real and sham dry needling applications will be performed under ultrasound guidance, with both the patient and the evaluator blinded. This study design has the potential to make a significant contribution to the literature in this field.
Trial Details
NCT Number NCT06338488
Lead Sponsor Kutahya Health Sciences University
Conditions
(from sponsor)
Shoulder Pain
Related terms Shoulder Pain
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov