Actively Recruiting
Percutaneous Electrolysis of the Upper Trapezius in Chronic Neck Pain
Led by Sivas State Hospital · Updated on 2025-12-19
40
Participants Needed
1
Research Sites
22 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In the planned study, we aim to investigate the effectiveness of percutaneous electrolysis treatment applied to myofascial trigger points in the upper trapezius muscle in patients with chronic neck pain. Two different protocols, a low-intensity (0.5 mA × 90 s) and a high-intensity (3 mA × 3 s × 3 repetitions), will be compared in the study. Patients participating in the research will be randomized into 2 groups using a computer program. Stretching exercises targeting the upper trapezius muscle will be given to both groups as a home exercise program. In both groups, the percutaneous electrolysis treatment protocol will be performed on the active myofascial trigger points in the upper trapezius muscle on the 1st, 8th, and 14th days of treatment, using 0.3-millimeter acupuncture needles and an EPTE® percutaneous electrolysis device (Ionclinics \& A. Deionic SL, Valencia, Spain). The low-intensity (0.5 milliampere × 90 s) treatment protocol will be applied to Group 1, and the high-intensity (3 milliampere × 3 s × 3 repetitions) treatment protocol will be applied to Group 2. In the study, two different protocols, low-intensity (0.5 mA × 90 s) and high-intensity (3 mA × 3 s × 3 repetitions), will be compared. In this way, it is aimed both to obtain information about optimal dosing and to contribute to the literature for a frequently involved muscle such as the upper trapezius.
CONDITIONS
Official Title
Percutaneous Electrolysis of the Upper Trapezius in Chronic Neck Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who agree to participate in the study
- Aged between 18 and 70 years
- Symptoms lasting at least 3 months
- Chronic neck pain with active myofascial trigger points in the upper trapezius muscle
You will not qualify if you...
- Malignancy
- Active infection
- History of widespread inflammatory rheumatic disease or fibromyalgia
- Trauma
- Skin lesions, infection, or open wounds at the myofascial trigger point region
- Coagulopathy or use of warfarin
- History of spinal or shoulder disorders
- Previous neck or upper extremity surgery
- Acute illness
- Muscle diseases
- Epilepsy
- Use of sedative medications
- Needle phobia
- Previous dry needling treatment for myofascial pain
- Cardiac pacemaker
- Metal implants in the treatment area
- Conditions that contraindicate physiotherapy such as pregnancy
- Metal allergy
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sivas Devlet Hastanesi
Sivas, Turkey (Türkiye)
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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