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The Effects of Laser Acupuncture

The Effects of Laser Acupuncture on Myofascial Pain Syndrome-a Randomised Controlled Trial on Female Subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190413043266N1
Enrollment
60
Registered
2019-07-01
Start date
2009-08-16
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Myofacial Pain Symdrome. Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention 1: Treatment group: Low-level laser (830 nm, 1.5 J, 30 mw) was applied on 13 Aqupuncture points (C7and SI3, LU7, GB21, GB34, GB39, UB10 bilaterally) with contact way. This group received

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients were only included if they had all or most well-identified symptoms of MPS in the neck. According to reliable rheumatology resources, these symptoms include pain, spasms, sensitivity to stress, active trigger point, joint stiffness, muscle weakness, and motor limitation In addition, the presence of active trigger points in the trapezius (upper fibers) was another necessity for entering the study

Exclusion criteria

Exclusion criteria: Patients were excluded if they had symptoms of fibromyalgia in physical examination Subjects with history of herniated discs, fractured neck or cervical vertebrae, surgery, radiculopathy, and myelopathy were also excluded Moreover, individuals who had taken non-steroidal anti-inflammatory drugs or pain killers during the two-week period prior to treatment were not included

Design outcomes

Primary

MeasureTime frame
Pain intensity during rest and exercise. Timepoint: Baseline, the 5th and 10th sessions, and one month after the treatment. Method of measurement: In order to measure pain intensity, the patients were asked to mark their pain during rest and exercise on a 10-cm linear visual analogue scale (VAS).;The range of motion. Timepoint: Baseline, the 5th and 10th sessions, and one month after the treatment. Method of measurement: The active range of motion of the neck using a goniometer.;Pressure sensitivity. Timepoint: Baseline, the 5th and 10th sessions, and one month after the treatment. Method of measurement: Pressure sensitivity was assessed using a mechanical pressure algometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSayed Mohsen Mirbod

Esfahan University of Medical Sciences

mirbod@rehab.mui.ac.ir+98 31 3792 5000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026