Overview

Exploration of Genotype Based Personalized Prescription of Valproate Sodium in Anti-epileptic Treatment

Status:
Unknown status
Trial end date:
2013-07-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to investigate the relationship between the side effects of valproate sodium in the treatment of epilepsy in Han Chinese and the genetic polymorphisms of drug metabolizing enzymes and pharmacokinetics of valproate sodium.
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sun Yat-sen University
Collaborator:
First Affiliated Hospital, Sun Yat-Sen University
Treatments:
Anticonvulsants
Valproic Acid
Criteria
Inclusion Criteria:

- The patients must have been diagnosed as epilepsy according to The International
League Against Epilepsy (ILAE) criteria published in 2001.

- The patients must sign the informed consent. And for the patients who are under 18
years old, both the signatures of their legal guardians and that of the patients are
required on the written informed consent.

- The patients are receiving the regimen of 15-30mg/kg valproate sodium given as daily
oral administration.

Exclusion Criteria:

- Pregnant women, women in breast-feeding period and the women who refuse to take
contraception measures during treatment.

- Patients with poor compliance.

- Patients who have blood transfusion during the therapy.