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Comparison of pulsed radiofrequency and joint injection with steroid for sacroiliac joint pain

Comparison of intra-articular pulsed radiofrequency by two needle technique and steroid injection for sacroiliac joint pain: a randomized, double-blind, pilot study

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045581
Enrollment
34
Registered
2022-09-16
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intra-articular pulsed radiofrequency of SIJ: 2 radiofrequency needles will be placed intra-articular in the SIJ under fluoroscopic guidance. Pulsed radiofrequency will be performed for

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Low back ache for more than 3 months with or without radiation to leg 2. Numerical rating scale (NRS) for pain greater than 4 on 11 point scale 3. 3 out of 6 provocative tests for SIJ pain must be positive. These include: FABER, Ganslenâ??s test, sacral thrust, SIJ compression, distraction and thigh thrust test 4. A positive response to diagnostic intra articular SIJ injection with local anesthetic. Patient must report pain relief more than 75% on NRS scale

Exclusion criteria

Exclusion criteria: Patient refusal Focal neurological signs or neuropathic pain Other cause of low back ache â?? radiculopathy, facet joint pain Allergy to contrast or local anesthetics Previous history of intervention for SIJ pain Pregnant patients Patients with inflammatory arthritis â?? ankylosing spondylitis, rheumatoid arthritis Bleeding or coagulation disorders Opioid addiction of psychiatric disorders

Design outcomes

Primary

MeasureTime frame
Numerical Rating Scale for painTimepoint: Pre Procedure at 7 days,15 days 1, 3 and 6 months post procedure

Secondary

MeasureTime frame
Oswestry disability index score, global perceived effect (GPE) and decrease in analgesic medication use.Timepoint: Pre Procedure at 7 days,15 days 1, 3 and 6 months post procedure

Countries

India

Contacts

Public ContactVirender Kumar Mohan

AIIMS, New Delhi

dr_vkmohan@yahoo.com9868397803

Outcome results

None listed

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