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The effect of pressure release,dry needling and therapeutic ultrasound on painful point of trapezius muscle in neck

The Comparison between the effect of Pressure Release, Phonophoresis and Dry Needling on treatment of latent Trigger Point of Upper Trapezius Muscle

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015103024729N1
Enrollment
60
Registered
2015-11-16
Start date
2013-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

myofascial trigger point of upper trapezius.

Interventions

Intervention 1: Pressure release: in this technique patients treat with manual pressure on trigger point of muscle. Intervention 2: Dry needling: in this technique trigger point of patient treat with
Treatment - Devices
Treatment - Other
Treatment - Drugs
Pressure release: in this technique patients treat with manual pressure on trigger point of muscle.
Dry needling: in this technique trigger point of patient treat with needle striking.
Phonophoresis: in this method betamethasone solution pass via skin by usage of ultrasonic waves.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were presence of tender spot within taut band in the upper trapezius muscle which was painful in response to 25 Newton (N) pressures on it. Exclusion criteria were diagnosis of fibromyalgia syndrome; history of whiplash; history of neck surgery; myofascial trigger point treatment at least during last past month; presence of cervical radiculopathy that determined by physician; presence of sever postural deviation such as scoliosis or hyper kyphosis; presence of active myofascial trigger point sign include jump sign; local hemorrhage; consumption any anticoagulation drug; usage alcohol or any material that disturb the consciousness of person.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cervical range of motion. Timepoint: Before and after the treatment. Method of measurement: Goniometry.;Pain intensity. Timepoint: Before and after the treatment. Method of measurement: Visual Analoge Sclae.;Pain pressure threshold. Timepoint: Before and after the treatment. Method of measurement: Algometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Tabatabaiee

Iran University of Medical Sciences

tabataba.a@tak.iums.ac.ir+98 21 2253 4001

Outcome results

None listed

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