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Effect of radial extracorporeal shockwave therapy for sciatic pain with disc herniation

Effect of radial extracorporeal shockwave therapy for sciatic pain with disc herniation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210112050014N1
Enrollment
28
Registered
2021-04-10
Start date
2021-02-15
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

sciatic pain resulting from disc herniation. Sciatica, unspecified side

Interventions

Intervention 1: treatment group (A) receive baseline treatment include moist hot packs for 10 minutes at lower back then apply mechanical traction for 10 minutes then do shockwave therapy at paraverte

Sponsors

The University of Faisalabad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 45 Years

Inclusion criteria

Inclusion criteria: Both males and females between the age of 30-45 years having low back pain patient with moderate to severe low back and buttock pain runs down to the leg and having positive straight leg raising test between the angle of 30 to 70 degree patients have numbness and weakness and feeling of pins and needles in affected leg and feet pain that worsen with movement chronic sciatic pain lasts for 1 to 3 months psychological stable patients

Exclusion criteria

Exclusion criteria: acute pain bilateral sciatica spinal fractures pregnancy previous history of any inflammatory disease presence of any implant epiphyseal plate in the area any malignant condition patients with fixed contractures in the lower limb patients having phobia with shockwaves

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pain will be measured at the time of initial assessment, then after two weeks and after fourth week. Method of measurement: Visual analogue scale consist of 0 to 10 numbering for measurement of pain intensity ask patients to select any number from 0 to 10.

Secondary

MeasureTime frame
Disability. Timepoint: Questioner will be used at the time of assessment then after two weeks and after fourth week. Method of measurement: The patient is instructed to put a mark next to each appropriate statement, at the beginning of treatment, a patient’s score was 12 and, at the conclusion of treatment, her score was 2 (10 points of improvement), we would calculate an 83% (10/12 x 100) improvement.

Countries

Pakistan

Contacts

Public ContactDr Nazia Sarfraz; PT

The University of Faisalabad

nazia.sarfraz@tuf.edu.pk+92 41 8868326

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026