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The effects of epidural steroid injectio

Phase 2
Conditions
recurrent lumbar discopathy.
nerve root and plexus
Registration Number
IRCT138903084047N1
Lead Sponsor
Kerman Neuroscience Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

recurrent disc herniation who do not respond to conventional treatment, radicular pain is greater than lumbar pain, 6 weeks past from pain onset
Exclusion criteria: severe extruded intervertebral disc, progressive neurological deficit, history of steroid injection for lumbar or radicular pain, financial or complaint gain, history of coagulopathy or allergy to anesthetic agent or corticosteroid, pregnancy

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of pain. Timepoint: 1, 2 & 6 months after the intervention. Method of measurement: numerical pain score.;Walking tolerance. Timepoint: 1, 2 & 6 months after the intervention. Method of measurement: meter.;Standing tolerance. Timepoint: 1, 2 & 6 months after the intervention. Method of measurement: minute.
Secondary Outcome Measures
NameTimeMethod
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