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A clinical trial to study the effect of slow and rapid withdrawal of antiepileptic drugs in patient with epilepsy in epilepsy monitoring unit

Not Applicable
Conditions
Health Condition 1: null- drug refractory epilepsy patient admitted in epilepsy monitoring unit
Registration Number
CTRI/2016/08/007207
Lead Sponsor
Prof Manjari Tripathi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
140
Inclusion Criteria

• Patients admitted in epilepsy monitoring unit (EMU)

•Patient giving consent

Exclusion Criteria

•Patient not giving Consent.

•Patients having history of status epilepticus and Seizure frequency more than 1/day

•Patient with significant non- neurological co-morbidities like chronic cardiac, renal and other systemic diseases.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Difference in the duration of long-term video-EEG completion time between rapid and slow AED taper groups.Timepoint: Time points will be calculated as total days patient admitted in epilepsy monitoring room.
Secondary Outcome Measures
NameTimeMethod
long term video-EEG diagnostic yield (calculated as a percentage of prerecording question answered upon completion of LTM) in both groupsTimepoint: Time points will be calculated as total days patient admitted in epilepsy monitoring room.;The percentage of patient with ictal onset EEG localization in two groupsTimepoint: Time points will be calculated as total days patient admitted in epilepsy monitoring room.;The percentage of secondary GTCS (sGTCS), 4-hr and 24-hr cluster, status epilepticus, need for midazolam rescue treatment and LTM associated complications in two groupsTimepoint: Time points will be calculated as total days patient admitted in epilepsy monitoring room;The time to first seizure in two groupsTimepoint: Time points will be calculated as total days patient admitted in epilepsy monitoring room.
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