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To Administer The Single Shot Epidural Injection In Patients With Prolapsed Intervertebral Disc

Effect Of Single Shot Epidural Injection In Patients With Prolapsed Intervertebral Disc (PIVD). - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064530
Enrollment
279
Registered
2024-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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: Single Shot Epidural Steroid Injection.: The study population includes all the PIVD patients who will be referred in pain opd from orthopedic and neurosurgery department during the

Sponsors

Dr.Anjali Panwar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 18–80 years 2 .Lumbar/Lumbosacral radicular pain/or low back pain that have not responded to conservative treatments (pharmacotherapy and physical therapy) . 3. Symptomatic patients with MRI proven disc prolapse at different level. 4. Patients who would be available for follow up for minimum of 1 month. 5. Chronic low backache with radiculopathy. 6. Patients willing for steroid injection.

Exclusion criteria

Exclusion criteria: 1. Patients not giving consent for the procedure. 2. Patients with neurological deficits. 3 .H/O Allergic reactions to local anaesthesia ,opiates ,contrast agents or steroids. 4.Patients with Extruded and sequestered discs. 5. Patients with associated listhesis, instability of the spine. 6.Any systemic infection or local infection at the injection site. 7.Coagulopathy and bleeding disorders. 8.Uncontrolled diabetes not on any medications

Design outcomes

Primary

MeasureTime frame
To access pain using VAS Score in patients with PIVD after single shot epidural injection (ESI).Timepoint: Follow up of the patients to be done after 7 days postoperatively.

Secondary

MeasureTime frame
1.To monitor haemodynamic parameters . 2 To observe for any side effects. Timepoint: Follow up of the patients to be done after 7 days postoperatively.

Countries

India

Contacts

Public ContactDr Geeta Bhandari

Government Medical College Haldwani

bhandari_geetantl@rediffmail.com8650655556

Outcome results

None listed

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