Skip to content

Comparison of the Effects of Needling and Shock Wave Therapy on Active Trigger Points

Effect of Dry Needling Versus Shock Wave Therapy on Pain and Dysfunction Following Active Trigger Points in Upper Trapezius Muscle

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190514043588N1
Enrollment
48
Registered
2019-12-29
Start date
2019-09-23
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Myofascial pain syndrome. Myalgia

Interventions

Intervention 1: Dry Needling : In this group, needle enters the upper trapezius muscle trigger point and stays in the muscle for 5 minutes. Two treatment sessions with a 48 hour interval during a week

Sponsors

Nikan hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age 18-35 Having active trigger points with a distinct bundle in the upper trapezius muscle Touch the Taut Band on the upper trapezius muscle fibers Pain above 3 and less than 7 on the VAS scale Pain for one to three months Having refferal pain

Exclusion criteria

Exclusion criteria: Performing injections or other treatments for trigger points during the research period Having a previous history of infectious diseases such as fibromyalgia and myopathy Malignancy or patients susceptible to infection Presence of central and peripheral neurological disorders Use of anticoagulants Having vascular diseases Fear Of Needle Skin ulcers in the treatment area

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: At baseline and immediately after the first session and after the second session. Method of measurement: Visual Analog Scale.;Pressure Pain Threshold. Timepoint: At baseline and immediately after the first session and after the second session. Method of measurement: Algometer.;Lateral bending Of Neck. Timepoint: At baseline and immediately after the first session and after the second session. Method of measurement: Goniometer.;Disability. Timepoint: Beginning and end of treatment. Method of measurement: Neck Disability Index Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehran Toghtamesh

Tehran University of Medical Sciences

mehrantoghtamesh@yahoo.com+98 21 2912 1018

Outcome results

None listed

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