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Investigation of the effects of intramuscular electrical stimulation on trigger points

A Comparative Study of Sonographic and Clinical Parameters of Trigger Point of the Upper Fiber of the Trapezius Muscle Following " Dry Needling " and " Intramuscular Electrical Stimulation " (IMES) through Needle.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170616034567N2
Enrollment
30
Registered
2020-09-11
Start date
2020-09-05
Completion date
Unknown
Last updated
2020-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Upper trapezius muscle trigger point.

Interventions

Intervention 1: Intervention group: intramuscular electrical stimulation, The intervention in this group was intramuscular electrical stimulation in which the patient was placed lying on his stomach.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Active trigger points in the upper trapezius muscle Pain associated with the upper trapezius muscle trigger point above 3 based on the VAS scale which is considered as moderate pain. Age: 18-35 years.

Exclusion criteria

Exclusion criteria: Perform injections or other treatments for trigger points in the period of one month before the research. Previous history of muscle diseases such as fibromyalgia and myopathy. Malignancy or patients prone to infection. Central and peripheral neurological disorders. Skin damage in the trigger point area. Taking sedatives before and during treatment. Radicular pain and history of neck and shoulder surgery. Previous history of bad response to acupuncture or dry needling. Pregnancy. Taking anticoagulants. Significant fear of dry needling. Vascular disease. Diabetes. History of migraine. History of accident or trauma in the relevant areas.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before, after and one month after treatment. Method of measurement: by Visual Analogue Scale.;Pain pressure threshold. Timepoint: Before, after and one month after treatment. Method of measurement: by algometer.;Neck range of motion. Timepoint: Before, after and one month after treatment. Method of measurement: lateral flexion and rotation by goniometer.;Disability. Timepoint: Before, after and one month after treatment. Method of measurement: by Neck Disability Index.;Ultrasonic parameters. Timepoint: Before, after and one month after treatment. Method of measurement: by sonography device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMonavar Hadizadeh

Shahid Beheshti University of Medical Sciences

Hadizadeh.mahsa1992@yahoo.com+98 21 7754 8496

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026