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Comparative study of radial shockwave therapy and high intensity laser therapy in the treatment of patients with myofascial pain syndrome in neck and upper back area

Comparative study of radial shockwave therapy and high intensity laser therapy in the treatment of patients with myofascial pain syndrome in neck and upper back area

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100127003217N15
Enrollment
40
Registered
2023-11-01
Start date
2023-10-23
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Myofascial pain syndrome. Other chronic pain

Interventions

Intervention 1: Intervention group: The first group, radial shock wave therapy (ESWT: Extracorporeal shock wave therapy) in 3 sessions, 2 sessions per week with an intensity of 0.2 mj/mm2, frequency o

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Acute or chronic pain in the neck and shoulder muscles The presence of trigger points and tight bands in the muscles around the neck and head more than 2 points The appearance of referred pain in the peripheral muscle in response to pressure on the trigger point

Exclusion criteria

Exclusion criteria: The presence of clear radiculopathy based on the history and the presence of one of the findings of radiculopathy in the form of weakness, radicular pain, or decreased reflexes, or upper limb sensation disorder, and a positive Spurling test The presence of extrude cervical discopathy proven in MRI The presence of severe cervical degenerative changes and the presence of radiculopathy History of cervical spine surgery or trauma Existence of systemic diseases such as bleeding disorders or rheumatological and cardiovascular diseases History of taking psychological drugs Pregnancy Malignancy

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before, immediately and 2 months after treatment. Method of measurement: Visual analogue scale ( VAS ).;Neck disability index (NDI). Timepoint: Before, immediately and 2 months after treatment. Method of measurement: Neck disability Index questionnaire.;Neck range of motion(ROM). Timepoint: bubble inclinometer. Method of measurement: Before, immediately and 2 months after treatment.;Pressure pain threshold (PPT). Timepoint: Before, immediately and 2 months after treatment. Method of measurement: Algometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHiva Shadmani

Tabriz University of Medical Sciences

H.shadmany@gmail.com+98 41 3336 1928

Outcome results

None listed

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