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The effects of non-surgical decompression in addition to routine physical therapy in patients with lumber radiculopathy; A Randomized Controlled Trial

The effects of non-surgical decompression in addition to routine physical therapy in patients with lumber radiculopathy; A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190717044238N1
Enrollment
60
Registered
2019-12-23
Start date
2018-10-20
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Lumber Radiculopathy. Radiculopathy, lumbar region

Interventions

Intervention 1: Control group: The control group will receive conventional physiotherapy including electrotherapy and trunk stability exercises. The treatment will be performed as follows:1) Electroth

Sponsors

The University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Both male and female patients Age between 25-55 years Clinically and radiologically diagnosed patients (by neuro-surgeon) of lumbar radiculopathy Radiating Low Back Pain for at least 3 months Willing to participate in the study

Exclusion criteria

Exclusion criteria: Recent fracture or dislocation of lumber vertebra History of surgery on lumber spine, hip or pelvis Spinal tumors or infections in the intervertebral disc Inflammatory diseases such as rheumatism Spinal deformity such as scoliosis Spondylolysthesis Osteoporosis below L1 Patients taking medications e.g NSAIDS for pain Severe disc degeneration Pregnant females Having three or more herniation

Design outcomes

Primary

MeasureTime frame
Pain Intensity. Timepoint: before intervention and after 4 weeks of intervention. Method of measurement: Visual Analogue Scale.;Lumber range of motion. Timepoint: before intervention and after 4 weeks of intervention. Method of measurement: Clinical Test (Modified-Modified Schober's Test).

Secondary

MeasureTime frame
Quality of Life. Timepoint: before intervention and after 4 weeks of intervention. Method of measurement: SF 36 scoring calculator will be used.;Level of disability. Timepoint: before intervention and after 4 weeks of intervention. Method of measurement: ODI scoring calculator.;Endurance. Timepoint: before intervention and after 4 weeks of intervention. Method of measurement: Stop Watch will be used to calculate the endurance time.

Countries

Pakistan

Contacts

Public ContactFareeha Amjad

The University of Lahore

fari_fairy22@yahoo.com+92 42 99200600

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 18, 2026