Skip to content

Stimulator-assisted ultrasound-guided nerve block versus ultrasound guided injection in low back pain relief

Comparison of efficacy of nerve stimulation-assisted ultrasound-guided transforaminal injection versus ultrasound-guided transforaminal injection in patients with lumbar radicular pain: A Randomized Interventional Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035926
Enrollment
40
Registered
2021-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Nerve stimulation-assisted ultrasound-guided transforaminal injection: Group N: Nerve stimulation-assisted ultrasound-guided transforaminal injection with 2 mL of 1% lidocaine with 4 mg

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Low back pain with unilateral radicular pain with clinical-radiologic signs without paresis 2) VAS >3 3) 18 to 65 year 4) Who gives informed consent to inclusion in the study 5) Who has current CT or MR imaging of their lumbar spine available 6) Monosegmental dermotomal pain distribution 7) Failure of symptomatic treatment with NSAIDs or/and physiotherapy for at least 6 weeks

Exclusion criteria

Exclusion criteria: 1) History of drugs allergy including contrast media, steroid and anaesthetics 2) Body mass index of >=35 kg/m2 3) Spinal infection or a local or systemic infection 4) Pregnant patient 5) Previous injections within 3 months 6) Uncontrolled diabetes 7) Spinal tumors 8) On anticoagulation therapy or uncorrectable coagulopathy 9) Underwent surgery in the lumbar region 10) Progressively neurological deficit, acute traumatic, infectious, or pathologic cases

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS)Timepoint: 1 month

Secondary

MeasureTime frame
1. Visual Analogue Scale (VAS) 2. Number of needle attempts between the two groups 3. Contrast spread pattern between the two groups 4. Operation time between the two groupsTimepoint: 30 mins, 1 week and 3 months

Countries

India

Contacts

Public ContactDr Jyotsna Punj

AIIMS, New Delhi

jyotsna_punj@yahoo.com9810191116

Outcome results

None listed

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