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Use of laser beams on postneedling soreness and treatment of chronic cervical pain

Short Term Effects of Low versus High Power Lasers on Soreness following Dry Needling at Neck Myofascial Pain Syndrome induced by Active Trigger Points of Upper Trapezius Muscle.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190411043241N1
Enrollment
45
Registered
2019-09-02
Start date
2019-06-30
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Active Trigger Points in Upper Trapezius Muscle.

Interventions

Intervention 1: Intervention group: High Power Laser: In this group, the dry needle is applied to the most active trigger point in the upper trapezius muscle. Immediately a laser with a power of 1 wat

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Females aged 18-35 years old Cervical pain lasting for 3 months or more Neck pain intensity of at least 3 points based on the VAS scale Presence of a palpable taut band in the muscle Presence of a hypersensitive tender spot in the taut band Local or referred pain elicitation in response to compression

Exclusion criteria

Exclusion criteria: Contraindications of dry needling(cancer, presence of coagulation and vascular disorders, Pregnancy, epilepsy, fibromyalgia, needle aversion or phobia) Significant psychological disorders Stress in the last week Cervical radiculopathy pain Dizziness History of cervical surgery

Design outcomes

Primary

MeasureTime frame
Pain of palpation. Timepoint: Before intervention, immediately after, 24 and 48 hours after intervention. Method of measurement: Visual Analogue Scale.;Pain Pressure Threshold. Timepoint: Before intervention, immediately after, 24 and 48 hours after intervention. Method of measurement: By using algometer.

Secondary

MeasureTime frame
General pain. Timepoint: Before intervention, immediately after, 24 and 48 hours after intervention. Method of measurement: Visual Analogue Scale.;Cervical range of motion. Timepoint: Before intervention, immediately after and 48 hours after intervention. Method of measurement: By using a goniometer.;Neck disability. Timepoint: Before intervention and 48 hours after intervention. Method of measurement: Neck Disability Index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Motavalian

Tehran University of Medical Sciences

m-motavalian@razi.tums.ac.ir+98 21 7753 3939

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026