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A study on new antiepileptic drug levetiracetam in patients with epilepsy surgery

Not Applicable
Recruiting
Conditions
epilepsy
Registration Number
JPRN-UMIN000006703
Lead Sponsor
Graduates School of Biomedical Sciences, Department of Neurosurgery, Hiroshima University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

Patients already administered levetiracetam before starting the test drugs. Patients with a history of hypersensitivity for ingredients of the test drugs or pyrrolidone derivatives. Patients with psychiatric disease, progressive neurological disorder and other serious complications. Patients during administering other investigational or unapproved drugs within three months before starting a follow-up. Patients with clinical trials of levetiracetam in the past. Patients with levetiracetam discontinued because of the side effects in the past. Patients with non (or potential of non)-compliance to regular medication or doctor consultation appointments. Pregnant or potentially pregnant women, breast-feeding women. Patients considered to be inappropriative for carrying out the trials by attending physicians.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ong-term tolerability of levetiracetam in patients with epilepsy surgery
Secondary Outcome Measures
NameTimeMethod
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