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A study to see the efficacy of pyriformis injection wth local anaesthetic plus steroids for management of pyriformis syndrome.

Role of pyriformis injection with local anaesthetic plus steroids for management of pyriformis syndrome: a study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009223
Enrollment
30
Registered
2017-08-02
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- Pyriformis syndrome

Interventions

Intervention1: Local anaesthetic plus steroids: 3 mL of 0.25% bupivacaine with 40 mg methyl prednisolone will be injected into pyriformis muscle under fluroscopic and nerve stimulator guidance. Contro

Sponsors

ESI Institute of Pain Management ESI Hospital Sealdah
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Pain -unilateral hip and/or leg pain with positive FAIR (flexion, adduction, internal rotation) test ii. Tenderness and/or trigger point at the Pyriformis Muscle iii. Pain unresponsive to conservative treatment like pharmacotherapy with nonsteroidal anti-inflammatory drugs, muscle relaxants, and neuropathic pain agents and physical therapy, which includes stretching of the pyriformis Muscle to correct the underlying pathology

Exclusion criteria

Exclusion criteria: i. Uncontrolled hypertension , uncontrolled diabetes mellitus ii. Patients having a neurological deficiency iii. Surgery involving lumbar and/ or hip region iv. History of allergic reaction to the drug and contrast agent to be used v. Patient on anticoagulant vi. History of inflammatory or infectious disease vii. Non-compensated chronic heart/liver/renal deficiency viii. Vascular/tumoral disease. ix. Gestational or lactational period.

Design outcomes

Primary

MeasureTime frame
Pain using Numerical Rating Score (NRS) on a scale of 1-10Timepoint: Just before the injection and one hour, one week and three weeks after giving the injection

Secondary

MeasureTime frame
Back Disability using the roland morris disability questionnaire on a scale of 0-24.Timepoint: Just before the injection and one hour, one week and three weeks after giving the injection

Countries

India

Contacts

Public ContactDr Subrata Goswami

ESI Institute of Pain Management

drsgoswami@gmail.com9830430430

Outcome results

None listed

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