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Effect of High Intensity Laser on Hemiplegic Shoulder Dysfunction

D

Deraya University

Status and phase

Completed
Phase 1

Conditions

Stroke
Shoulder Dislocation or Subluxation

Treatments

Device: hight intenisty laser

Study type

Interventional

Funder types

Other

Identifiers

NCT05595720
Deraya U

Details and patient eligibility

About

Hemiplegic shoulder pain (HSP) is a common and disabling complication following a stroke, and it may affect the quality of life. It often occurs following two to three months of stroke. Upper limb impairment is seen in 90% of patients affected by stroke.

Numerous causes have been implicated in developing HSP in stroke. This includes muscle flaccidity around the shoulder joint, shoulder subluxation, shoulder-hand syndrome, increased muscle tone, impingement syndrome, frozen shoulder, brachial plexus injury, and the thalamic syndrome.

Muscle paresis, abnormal muscle tone and loss of proprioception following stroke may render the shoulder complex unstable and therefore prone to misalignment.

In recent years, high-intensity laser therapy (HILT) has been considered as a treatment option for shoulder pain.

HILT increases microcirculation and tissue regeneration and lowers edema, inflammation, and pain with its photomechanical, thermal, electrical, and bio stimulating effects in deep tissues that cannot be reached with LILT.

It has some advantages over LILT, i.e., having higher power, greater tissue penetration capacity to deep tissues, the short emission time, and long rest periods preventing heat accumulation.

In recent studies, effectiveness of HILT has been shown in the treatment of subacromial impingement syndrome, rotator cuff tendinopathy, and frozen shoulder.

Enrollment

44 patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • DISORDER MORE THAN 6 MONTHS
  • UNILATERAL
  • FIRST TIME

Exclusion criteria

  • Iinflammatory rheumatic disease,
  • cervical radiculopathy,
  • diabetes mellitus,
  • thyroid disease,
  • coronary heart disease,
  • cardiac pacemaker,
  • neurological disease,
  • shoulder surgery, and
  • shoulder injection in the last 3 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

44 participants in 2 patient groups

treatment group
Experimental group
Treatment:
Device: hight intenisty laser
control group
No Intervention group

Trial contacts and locations

1

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Central trial contact

MAGDY M SHABANA, PH D; Soad A. Mohamad

Data sourced from clinicaltrials.gov

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