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Contrast pattern comparison of two approaches of transforaminal injection

Contrast volume needed to reach anterior epidural space via Kambins triangle or subpedicular approach for transforaminal epidural injection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011168
Enrollment
75
Registered
2018-01-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: null- chronic low back pain with radicular pain showing more than 5 on Numerical Rating Scale (NRS) Health Condition 2: G541- Lumbosacral plexus disorders

Interventions

Intervention1: Group KT: Patients in this group will receive transforaminal epidural injection using Kambins Triangle approach of transforaminal procedure at selected site. Control Intervention1: Grou

Sponsors

PGIMER Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient of ASA1 and ASA2 of either gender between 18 to 65 yrs of age having unilateral low back pain and / or unilateral radicular lumbar pain =3 months which will not responding to non invasive conservative management with Numerical Raging Scale = 5 requiring epidural injection.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to contrast 2. Patient with previous h/o surgery of spine 3. Patient who had received TF epidural injection in past 4. Patient having cutaneous disorder around the injection site 5. Mentally retarded 6. Patient with cauda equine syndrome 7. Patient on systemic steroid 8.Pregnancy

Design outcomes

Primary

MeasureTime frame
To determine the volume of contrast needed to reach Anterior Epidural Space via Kambins triangle and subpedicular approachTimepoint: While doing the intervention procedure on operation table

Secondary

MeasureTime frame
.To evaluate the contrast spread medial to inferior pedicle of the corresponding level of injection. 2. To evaluate the contrast spread medial to superior pedicle of the corresponding level of injection. 3.Pain relief over follow up times Timepoint: 2 week, 4 week and 8 week

Countries

India

Contacts

Public ContactDr Amit Gupta

Post Graduate Institute of Medical Education and Research

ghaibabita1@gmail.com7087009533

Outcome results

None listed

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