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Effect of different doses of steroid on pain relief in patients receiving injections in back for pain

Effect of different doses of dexamethasone on pain relief in patients receiving fluoroscopic guided parasagittal inter laminar epidural steroid injection for low back pain with radicular leg pain

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/07/014780
Enrollment
60
Registered
2018-07-09
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: null- Low back pain with unilateral lumbosacral radicular pain of at least 3 months duration not responding to medications and physical therapies. Health Condition 2: M248- Other specific joint derangements,not elsewhere classified

Interventions

Intervention1: Group A: Patients in this group received a dose of 12mg of Dexamethasone (total volume of 6 ml). Injection will be repeated at an interval of 15 days in patients having less than 50% pa

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: History of low back pain with unilateral lumbosacral radicular pain of at least 3 months duration not responding to medications and physical therapies. Radicular pain was defined as sharp, shooting or lanceting pain perceived in skin and deep dermatomal level

Exclusion criteria

Exclusion criteria: Patient with history of Surgery on lumbar spine Spinal canal stenosis Facet joint arthropathy Allergic to contrast or steroid Bleeding diathesis Patient who received lumbar epidural steroid injection in past three months using systemic steroid for pain relief. Pregnant patient.

Design outcomes

Primary

MeasureTime frame
To compare the effect of different doses of lumbar epidural dexamethasone injection (12mg, 16 mg and 20 mg) on therapeutic efficacy in patients with lumbosacral radicular pain defined as number of patients receiving more than 50% pain relief at the end of 6 monthsTimepoint: 2 weeks, 1 month, 2month, 3 months and 6 months

Secondary

MeasureTime frame
Pattern of spread of iodinated contrast on fluoroscopy (unilateral or bilateral, anterior or posterior, caudal or cranial). Visual Analogue Scale (VAS) scores Modified Oswestry Disability Questionnaire (ODQ). Timepoint: 2 weeks, 1 month, 2month, 3 months and 6 months

Countries

India

Contacts

Public ContactDr Bijay KC

Post Graduate Institute of Medical education & Research

jeet1516@gmail.com7087009510

Outcome results

None listed

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