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Comparison of the effect of neurodynamic mobilization and dry needling techniques in patients with lumbar herniated disc

Comparison of the effect of neurodynamic mobilization and dry needling techniques on the pain, function, and ankle range of motion in patients with lumbar herniated disc

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240211060958N3
Enrollment
80
Registered
2024-12-31
Start date
2025-02-08
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

lumbar disc herniation. Connective tissue and disc stenosis of intervertebral foramina of lumbar region

Interventions

Intervention 1: Intervention group: Dry needling. The treatment is done in 3 sessions with an interval of one day. The muscles selected for dry needling in this study are practically important in the

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 50 Years

Inclusion criteria

Inclusion criteria: All participants are aged from 21 to 50 years A disc lesion is diagnosed with confirmation from an MRI and a specialist. Complaints of pain , numbness, and tingling along the path of the sciatic nerve for at least twelve weeks to a year and not having acute pain in the last 4 weeks Positive Slump and SLR tests with neurological symptoms. Having functional disabilities including lifting objects or walking.

Exclusion criteria

Exclusion criteria: Patients with sciatica due to other pathologies, such as lumbar canal stenosis or piriformis syndrome. After any spinal surgery, for example, unilateral hemilaminectomy or microdiscectomy. Patients with a negative Slump test and progressive neurological symptoms, e.g. hyperexcitability and instability. History of fracture or trauma to the vertebrae. Systemic disorder, for example diabetes.

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before, After and 1month follow up. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Functional index. Timepoint: Before, After and 1month follow up. Method of measurement: Oswestry Disability Index, Roland–Morris Disability and Quebec Back Pain Disability Scale questionnaires.;Ankle range of motion. Timepoint: Before, after and 1month follow up. Method of measurement: Goniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public Contacttahereh rezaeian

Kerman University of Medical Sciences

tahere.rezaiyan@gmail.com+98 34 3132 5700

Outcome results

None listed

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