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High Intensity Laser Versus Ischemic Compression on Myofascial Trigger Points in the Upper Trapezius

Cairo University (CU) logo

Cairo University (CU)

Status

Active, not recruiting

Conditions

Neck Pain

Treatments

Device: TENs , ultrasound therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06552780
012\005287

Details and patient eligibility

About

TO Investigate the effect of high intensity laser versus ischemic compression on myofascial trigger points on neck pain, cervical range of motion,pressure pain thershold and cervical disability and to show that the more effectivness therapy will provide significant clinical value

Full description

Randomized controlled Trial , participants will be assigned into three groups (study group A ,study group B and study group c ) Subject selection will be 63 subjects , 21 subjects in each group with trigger points in the upper trapezius.

Groups

Enrollment

63 estimated patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The age of patients range from 20 to 50 years .
  • patient Body mass index starting from 19 to 25 kg\m.
  • presence of myofascial trigger points in the shortened upper trapezius muscle evaluated .

Exclusion criteria

  • patients with fibromyalgia syndrome.
  • cancer or tumor or any type diagnosed .
  • patients with disc herniation or spinal canal stenosis.
  • pregnancy -
  • patients diagnosed with epilepsy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

63 participants in 3 patient groups

high intensity laser , TENs and ultrasound and isometric exercise
Experimental group
Description:
Group A ( study group )will receive high intensity laser ,TENs , ultrasound therapy , and isometric exercise.
Treatment:
Device: TENs , ultrasound therapy
ischemic compression ,TENs , ultrasound and isometric exercise
Experimental group
Description:
Group B ( study group) will receive ischemic compression ,TENs and ultrasound therapy and isometric exercise.
Treatment:
Device: TENs , ultrasound therapy
TENs , ultrasound and isometric exercise
Experimental group
Description:
Group C (control group ) will receive TENs and ultrasound therapy and isometric exercise only.
Treatment:
Device: TENs , ultrasound therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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