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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05320601
Other study ID # AIamchaimongkol
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 11, 2022
Est. completion date July 1, 2022

Study information

Verified date July 2022
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare efficiency between repetitive peripheral magnetic stimulation and dry needling in patient with upper trapezius myofascial pain syndrome.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date July 1, 2022
Est. primary completion date May 1, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: - Patients with myofascial pain syndrome at unilateral upper trapezius muscle and had pain score (Visual analog scale) at least 4 Exclusion Criteria: - Patients with signs and/or symptoms of neurological deficit - Patients with history of cervical hernia, cervical radiculopathy, cervical myelopathy, fibromyalgia, whiplash spondylosis and cervical spinal stenosis. - Patients who received physical therapy/injection/surgery at neck or pain area in last 6 months. - Patients with abnormal coagulopathy and/or currently use anticoagulant medicine. - Patients with cardiac device. - Patients with history of aneurysm clip procedure, stent-coils procedure or cochlear implant surgery. - Pregnancy

Study Design


Intervention

Device:
Repetitive Peripheral Magnetic Stimulation
Repetitive Peripheral Magnetic Stimulation at trigger point of upper trapezius muscle
Procedure:
Dry needling
Dry needling at trigger point of upper trapezius muscle

Locations

Country Name City State
Thailand Physical medicine and rehabilitation Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Other Pain pressure threshold The minimum pressure that induces pain in trigger point. Higher scores mean better outcome. Change from baseline Pain pressure threshold at immediately after intervention, Change from Baseline Pain pressure threshold at 1 week and Change from baseline Pain pressure threshold at 4 weeks
Primary Change of Visual analog scale Pain measurement Score from 0-10, 0 means no pain and 10 means maximum pain. Higher scores mean worse outcome. Change from baseline Visual analog scale at immediately after intervention, Change from Baseline visual analog scale at 1 week and Change from baseline Visual analog scale at 4 weeks
Secondary Neck disability index Disability secondary to neck pain Score from 0-50, 0 means no disability and 50 means complete disability. Higher scores mean worse outcome. Change from baseline Neck disability index at immediately after intervention, Change from Baseline Neck disability index at 1 week and Change from baseline Neck disability index at 4 weeks
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