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To compare the efficacy of 2 standard anti-epileptic drugs valproate and levetiracetam in status epilepticus among elderly

To compare the efficacy of sodium valproate (SVA) and levetiracetam (LVM) following initial lorazepam in convulsive status epilepticus in elderly: A prospective randomized study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/05/006932
Enrollment
100
Registered
2016-05-13
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- Patients with status epilepticus

Interventions

Intervention1: Sodium Valproate (SVA) (group 1): SVA will be compared against LVM SVA group will receive sodium valproate 25 mg/kg IV in 100 mL saline infused at speed of 6mg/kg/min over 15 minutes fo

Sponsors

NON FUNDED
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients with GCSE (more than 10 minutes of continuous convulsive seizure activity or two or more sequential seizures without full recovery of consciousness in between seizures), irrespective of etiology. • Willing to participate. • Age group more than 60 years.

Exclusion criteria

Exclusion criteria: • Not willing accompanying relatives/friends • Patients having non-convulsive SE • Liver failure, renal failure, cardiac disease (based on clinical judgment, available lab reports, ECG at presentation) • Requiring urgent neurosurgical intervention. • H/O allergy to drugs

Design outcomes

Primary

MeasureTime frame
Control of seizuresTimepoint: Control of seizures will be assessed in each subjects as soon as the study drug infusion is over. Subject will be continuously reassessed till primary outcome is arrived at.

Secondary

MeasureTime frame
Mortality and MorbidityTimepoint: Recruitment to 1 month

Countries

India

Contacts

Public ContactSANJIB SINHA

NIMHANS

sanjib_sinha2004@yahoo.co.in

Outcome results

None listed

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