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pregabalin in childhood eoilepsy

Not Applicable
Conditions
Seizure.
Attack with loss of consciousness
Registration Number
IRCT2014012216320N1
Lead Sponsor
Qom University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Inclusion critria: all patients with refractory seizure
Exclusion criteria: patients with myoclonic siezures; sensitivty to PGB; patients that recieved gabapentin.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Decrease count of seizure. Timepoint: One and four mounth after intervention. Method of measurement: Counting.;Decrease intensity of seizure. Timepoint: One and four month after intervention. Method of measurement: Asking from parents.
Secondary Outcome Measures
NameTimeMethod
Drug reaction. Timepoint: One and four month after interventionque. Method of measurement: Quetionair.
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