myofascial pain trigger point at the upper trapezius muscle myofascial pain syndrome, dry needling, acupuncture, trigger point, office syndrome, post-needling soreness, peripheral magnetic stimulation
Conditions
Interventions
Standard mode Normal current direction
Biphasic waveform Inter pulse interval 10msec
Burst pulse 2 Pulse B/A ratio 1.0
Repetitive rate 20 pulses per seconds pulse in train 20
Total
minimal intensity that visible muscle contraction
, Standard mode Normal current direction
Biphasic waveform Inter pulse interval 10msec
Burst pulse 2 Pulse B/A ratio 1.0
Repetitive rat
repetitive peripheral magnetic stimulation ,repetitive peripheral magnetic stimulation
Sponsors
Panyananthaphikkhu Chonprathan Medical Center Srinakharinwirot University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Patients with myofascial pain syndrome of the upper trapezius muscle with at least one myofascial pain trigger point treated by Deep Dry Needling Muscle and twitching were recorded using ultrasound and recorded in the form of a video clip. 2. Body mass index 19 to 25 kg/m2.
Exclusion criteria
Exclusion criteria: 1. Patients with metal magnets within the head or treatment area within 30 cm, such as sutures, clips, coils, magnetic dental implants or implanted insulin pumps. 2. Patients with digital therapeutic tools such as pacemakers, implantable cardioverter-defibrillators, vagus nerve stimulators [VNS] and wearable cardioverter-defibrillators. 3. Patients with a history of seizures or uncontrolled seizures. 4. Pregnant women 5. patients with severe or recent heart disease 6. History of treatment with repetitive peripheral magnetic stimulation (rPMS) 7. Have a history of taking painkillers anti-inflammatory drugs and muscle relaxants within 24 hours 8. Have a bleeding disorder such as haemophilia or take blood-thinning medication. (anticoagulant) 9. Has a fear of needles 10. Abnormal skin conditions at the acupuncture site, such as rashes, dermatitis, or infection 11. Allergies to disinfectants used to clean the skin, such as alcohol or povidone-iodine. 12. Allergic to needles or metal 13. Allergic to adhesive plaster or Tegaderm
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain pressure threshold Immediately after completed of the intervention Commander Algometer | — |
Secondary
| Measure | Time frame |
|---|---|
| Numeric rating scale 48 hours after completed intervention pain score | — |
Countries
Thailand
Contacts
Public Contactchomkajee sukareechai
Panyananthaphikkhu Chonprathan Medical Center Srinakharinwirot University
Outcome results
None listed