Health Condition 1: G719- Primary disorder of muscle, unspecified
Conditions
Interventions
Intervention1: Intervention: platelet rich plasma
Dose:4ml
Frequency: single injection
Route: Transforaminal epidural injection
Total Duration : single injection during study period
: Comparison of
Sponsors
Department of Anaesthesiology
Operation Theater
Eligibility
Inclusion criteria
Inclusion criteria: Patients giving written consent will be taken Patient in the age group of 20 to 60 years. ASA grade I & II Low back pain more than 3 months and unilateral lower limb with radicular pain Posterolateral lumbar disc herniation of L4/L5 or L5/S1 segment on CT and corresponding clinical symptoms and signs Pain level on VAS =5 No symptoms of severe nerve damage include motor paralysis, muscle atrophy and cauda equine syndrome No history of spinal surgery
Exclusion criteria
Exclusion criteria: ASA grade III to IV Infection Prior epidural injection in the past 3 months, such as nerve root injection and caudal injection Spinal tumors or tuberculosis Multi-segmental lumbar disc herniation, spinal deformity, or spinal stenosis • Allergic to the drug used in this study • Symptoms of severe nerve damage including motor paralysis, muscle atrophy, and caudaequina syndrome.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare pain relief with PRP Vs Triamcinolone in transforminal epidural for radicular pain due to lumbar disc herniation via VASTimepoint: Measurements of VAS and Likert score from 0 wk,1 wk,2wk, 1 month and 3 month | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare patients satisfaction with PRP vsTriamcinolone To compare safety & side effects of PRP vsTriamcinolone Timepoint: 12 weeks | — |
Countries
India
Contacts
Public ContactProf Sarita Singh
King Georges Medical University Lucknow
Outcome results
None listed