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Comparison of the effect of lumbar spinal nerve root block by transforminal and codal method on nerve involved in low back pain

The comparison of targeted spinal nerve root blockade with caudal vs transforaminal approach in lumbar radiculopathy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20111102007984N31
Enrollment
50
Registered
2022-01-14
Start date
2022-02-20
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Lumbar spinal nerve root block, Transforminal, Kudal, Lumbar radiculopathy. Low back pain

Interventions

Intervention 1: Intervention group: Intervention group: In Transforaminal group, blunt curved tip Racz needle G21 is introduced for each involved levels, under transverse process and pedicle conjuncti

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Radicular unilateral or bilateral low back pain more than six months Maximum two levels involved Age 40 to 70 years Lack of response to conservative therapy after three months ASA I-II Moderate to sever pain (VAS > 3)

Exclusion criteria

Exclusion criteria: Severe spinal deformity Spinal tumors Spine fracture Vertebral list?sis more than G II Local or systemic infection Taking anticoagulants Drug abuse History of allergic reaction to the studied drugs History of severe psychological disorders Pregnancy and lactation Severe or sudden onset of neurological complications such as urinary or fecal incontinence BMI>35 Patient refusal MRI contraindication such as pacemakers, defibrillators, aortic aneurysm clips Respiratory incompetence cause prone position intolerance Smoking or alcohol consumption History of lumbar spine surgery Peripheral neuropathy such as diabetes

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale. Timepoint: Before, two weeks and one month, and three months after the procedure. Method of measurement: based on questionnaire.

Secondary

MeasureTime frame
Oswestry Disability Index. Timepoint: One, and three months after the procedure. Method of measurement: Based on the questionnaire.;The amount of analgesia consumption. Timepoint: One, and three months after the procedure. Method of measurement: Record and take notes.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnad Imani

Iran University of Medical Sciences

farnadimani@yahoo.com+98 21 6651 5758

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026