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Efficacy of platelet rich plasma versus steroid infiltration of low back pain

Efficacy of Platelet-rich plasma vs Steroid Infiltration in management of Low Back Pain: A prospective randomized control study - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083608
Enrollment
55
Registered
2025-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: - Health Condition 2: M45-M49- Spondylopathies

Interventions

Intervention1: Platelet rich plasma: 1 dose of Platelet rich plasma would be injected at the facet joint, of patient having low back ache at the time of surgery. Follow up will be done at 1 week, 1 mo

Sponsors

Datta Meghe Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All Skeletally matured patients with either sex. Continuous or intermittent LBP for at least 3 months.

Exclusion criteria

Exclusion criteria: Skeletally immature patients. Patient with infection, traumatic spine injuries, spinal tumours, spinal deformities, and congenital spinal anomalies. Pregnant women or women who are breast feeding. Operated cases of spinal fusion surgery.

Design outcomes

Primary

MeasureTime frame
Reduction in pain at facet joint after platelet rich plasma injection as compared to steroid injection .Timepoint: Assessment will be done at 1 week ,1 month ,2 month ,3 month ,6 month

Secondary

MeasureTime frame
Reduction in Oswestry Low back disability score after platelet rich plasma injection as compare to steroid injectionTimepoint: Assessment will be done at 1 week , 1 month ,2 month ,3 month ,6 month

Countries

India

Contacts

Public ContactDr Rohit Randad

Datta Meghe Institute of Higher Education and Research

svd1111@gmail.com9860452519

Outcome results

None listed

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