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To study effect of ketamine and clonidine when used with triamcinolone in chronic low back pain patients.

A placebo controlled study to compare efficacy of epidural ketamine and clonidine when used in combination with triamcinolone for chronic low back pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012872
Enrollment
90
Registered
2018-03-26
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- chronic low back ache

Interventions

Intervention1: epidural injection: epidural steroid injections with either ketamine 50 mg or clonidine 75 microgram to be given in 60 patients with chronic low back ache with placebo group of 30 patie

Sponsors

Sri Guru Ram Das Institute of Medical Sciences and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients - sensory deficit without any major motor component - age group 18 to 70 years - history of low backache with or without radiculitis of minimum 3 months duration and -no relief with conservative treatment will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Contraindications to epidural anaesthesia, such as local infections, generalised septicaemia, platelet and clotting factor abnormalities, significant neurological disease with motor or sensory deficit, diagnosed increased intracranial pressure 2. Contraindications to epidural ketamine like h/o psychiatric disorder, raised intracranial or intraocular pressure, h/o cardiovascular disorder or uncontrolled hypertension. 3. Contraindications to epidural clonidine like history of cardiovascular disease, history of postural hypotension or history of any psychiatric disorder. 4. A known history of allergy, sensitivity or any other form of reaction to local anaesthetics of amide type or opioids. 5. Psychiatric history or any other concomitant disease which may lead to unreliability. 6. Patients with spinal cord deformities like scoliosis, kyphosis in whom there is anticipated difficult epidural anaesthesia. 7. LESI done before enrolling patient for study 8. H/o spinal surgery 9. Caudaequina syndrome 10. Epidural lipomatosis 11. Opioid habituation 12. Pregnancy

Design outcomes

Primary

MeasureTime frame
Relief of pain from baselineTimepoint: 50 percent pain relief from baseline at 3 months follow up

Secondary

MeasureTime frame
Reduction in number of repeat blocksTimepoint: reduction in number of repeat blocks at 3 months follow up

Countries

India

Contacts

Public ContactDr Tavleen Kaur

Sri Guru Ramdas Institute Of Medical Sciences And Research Vallah Amritsar

shubhdeep999@yahoo.co.in8847271789

Outcome results

None listed

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