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Effect of High Versus Low-level Laser Therapy in Patients of Lumber Radiculopathy

Effect of High Versus Low-level Laser Therapy in Patients of Lumber Radiculopathy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06240845
Enrollment
38
Registered
2024-02-05
Start date
2023-08-01
Completion date
2023-10-10
Last updated
2024-02-05

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

Conditions

Lumbar Radiculopathy

Keywords

HLLT, Laser therapy , LLLT, Lumber radiculopathy, Sciatica

Brief summary

To Compare the effects of high-level laser therapy (HLLT) and low-level laser therapy (LLLT) on pain in patients with lumbar radiculopathy.

Interventions

This group received High-level laser therapy along with conventional physiotherapy treatment 3 times per week for 6 weeks.

OTHERLow-level laser therapy

This group received Low-level laser therapy along with conventional physiotherapy treatment 3 times per week for 6 weeks.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients of both genders male and female will be included. * Patients aged 40-65 years will be included. * Patients with a diagnosis of lumbar radiculopathy confirmed by clinical evaluation by a physician or physiotherapist. * Patients with a history of radicular leg pain and/or numbness or tingling sensation in the leg. * a positive score on the Straight Leg Raise (pain between 35 degrees and 75 degrees), pain limiting functional ability, and scores at least 3/10 on the VAS, restricted lumbar range of motion - 25% flexion, 20% extension. * Patients who have not received any form of treatment for lumbar radiculopathy within the past 3 months

Exclusion criteria

* Patients with a history of spinal surgery in the last 2 years or spinal deformity. * Patients with a history of fracture or dislocation of the lumbar spine. * Patients with a diagnosis of any other neurological disorder or neuropathy. * Patients who are pregnant or breastfeeding. * Patients with any other medical condition that may interfere i.e. inflammatory rheumatic disease, cardiac pacemaker, continuing that may interfere with the study outcomes or put them at risk with the study outcomes or put them at risk.

Design outcomes

Primary

MeasureTime frameDescription
Pain Level6 weeksVisual Analogue scale
Rang of motion6 weeksStraight Leg Raise
Level of Disability6 weeksOswestry Disability Index (ODI)
To measure Quality of Life6 weeksHealth Questionnaire (EQ-5D-5L)

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026