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Compare Effects of Ultrasound Therapy With High Intensity Laser Therapy for Treatment of Lumbar Disc Herniation.

Not Applicable
Completed
Conditions
Disk Herniated Lumbar
Interventions
Other: High Intensity Laser Therapy
Other: Ultrasound Therapy
Registration Number
NCT05261815
Lead Sponsor
Riphah International University
Brief Summary

The aim of this study is to assess and compare the effects of ultrasound therapy and High Intensity Laser Therapy, as the treatment option in case of lumbar disc herniation.

Detailed Description

A randomized control trail will be conducted in Safi teaching hospital near Riphah international university, after approval of synopsis. To evaluate the comparison and effect of Ultrasound therapy and High Intensity Laser Therapy, 30 patients will be randomly assigned to High Intensity Laser Therapy and Ultrasound group. Patients will be selected according to predefined inclusion and exclusion criteria. All the patients will be evaluated by computed tomography scan or magnetic resonance of lumbar spine. Non-probability convenient sampling will be used to approach the patients in hospital. Participants received 15 treatment session of High Intensity Laser Therapy and Ultrasound therapy over a period of three consecutive weeks (five days/week). Two types of tools will be used to evaluate the find out the comparison of both groups Visual analog scale and Oswestry lowback pain disability questionnaire. Data will be collected pre-treatment and post-treatment after 15 days. Data will be analyzed by Statistical Package of Social Sciences Version 20. Difference between pre-treatment to post treatment between group will be analyzed by Mann-Whitney test, and Within group difference will be analyzed by Wilcoxon signed- rank test. The level of statistical significance will be set as p\< 0.05

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patient above age 18 and adult
  • Patient with lumbar disc herniation diagnosed by MRI
  • Patient with no history of trauma and congenital abnormalities
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Exclusion Criteria
  • If patient received anesthesia or corticosteroid within 4 week
  • Patient with osteoporosis
  • Patient with surgery or previous fracture of spinal stenosis
  • A history of acute trauma like osteoarthritis, myofascial pain syndrome, inflammatory rheumatic disease, systemic lupus erythematosus, diabetes mellitus type 1 and 2, thyroid dysfunction, obesity, pacemaker, neurological pathologies and anxious- depressive syndrome.
  • Pregnant women
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
High Intensity Laser TherapyHigh Intensity Laser Therapy* High intensity laser for 10 minutes * Traction for 30 minutes * Spinal decompression exercises for 20 min
Ultrasound therapyUltrasound Therapy* Continuous ultrasound therapy for 15 minutes * Traction for 30 minutes * Spinal decompression exercises for 20 min
Primary Outcome Measures
NameTimeMethod
Visual Analogue Scale12th Week

A Visual Analogue Scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms.

Oswestry low back pain questionnaire12th Week

The Oswestry Low Back Pain Disability Questionnaire is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability. The test is considered the 'gold standard' of low back functional outcome tools

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ripah International University

🇵🇰

Faisalabad, Punjab, Pakistan

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