Pharmacogenetics-Based Study on Individualized Use of Sodium Valproate

NCT ID: NCT07046676

Last Updated: 2025-07-10

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE4
• Total Enrollment: 312 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-12-01
• Study Completion Date: 2026-05-30

Brief Summary

Sodium valproate (VPA) is a first-line prescription drug widely used in the treatment of epilepsy. However, in clinical applications, it has been found that there is a large individual variation in the blood concentration of VPA. In particular, excessively high blood drug concentrations can lead to various side effects, especially hepatotoxicity. Blood drug concentration monitoring can reduce the toxic and side effects of VPA to a certain extent and improve its effectiveness, but it is too cumbersome. A large number of studies have shown that the efficacy and toxic side effects of VPA are closely related to its in vivo metabolism process. The in vivo metabolism of VPA is affected by many factors, and the genetic polymorphism of drug-metabolizing enzymes is an important factor leading to differences in blood drug concentrations and affecting the dosage of VPA. The three products generated by the biotransformation of VPA by CYP450 enzymes are all related to hepatotoxicity. The formation of 4-ene-VPA is largely catalyzed by CYP2C9 and CYP2A6. Mutations in the CYP2A6 gene may be related to VPA hepatotoxicity, but there is a lack of further direct evidence. 50% of VPA in the body is acidified and metabolized into inactive products by uridine diphosphate glucuronosyltransferase (UGT) through phase II conjugation reactions. However, there is evidence that the genetic polymorphism of UGT can significantly affect the blood drug concentration of metformin. Based on the above research, we selected CYP2A6, UGT1A6, etc. as candidate genes, and studied the impact of genetic polymorphisms on the individual differences of sodium valproate through association analysis, with the hope of establishing a genetic model for optimal dosage and providing new strategies for the individualized use of VPA.

Conditions

Epilepsy

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Sodium valproate

According to the dosage forms of sodium valproate, they are divided into the sodium valproate tablet group, the sodium valproate oral solution group and the sodium valproate sustained-release tablet group.

Group Type: EXPERIMENTAL

sodium valproate

Intervention Type: DRUG

All three groups are administered twice a day via oral administration. Patients are given different doses based on their body weight and the therapeutic effect in controlling epilepsy.

Interventions

sodium valproate

All three groups are administered twice a day via oral administration. Patients are given different doses based on their body weight and the therapeutic effect in controlling epilepsy.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients diagnosed with epilepsy (primary epilepsy, secondary epilepsy) and with complete clinical data
• Regular use of valproic acid sodium for at least 5 days (with blood drug concentration reaching a steady state) and strong medication compliance
• Patients using combined anti-epileptic drugs or using valproic acid sodium alone
• Patients without significant liver or kidney dysfunction, and not in the pregnancy period

Exclusion Criteria

• Patients with incomplete data, poor compliance, and those whose blood drug concentration was not measured at the correct concentration
• Patients with major respiratory, gastrointestinal, liver, kidney or other serious diseases
• Patients using valproic acid solely for epilepsy prevention
• Patients who have used valproic acid for more than 5 days but have frequently changed the dosage form during the process
• Patients over 65 years old and in the 1CU

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The First Affiliated Hospital of University of South China

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The First Affiliated Hospital of University of South China

Hengyang, Hunan, China

Site Status: RECRUITING

Countries

China

Central Contacts

Jiecan Zhou, Prof.

Role: CONTACT

zhoujiecan@fsyy.usc.edu.cn

+86-734-8279018

Facility Contacts

Jiecan Zhou, Prof.

Role: primary

zhoujiecan@fsyy.usc.edu.cn

+86-734-8279018

Other Identifiers

nhfy20250317

Identifier Type: -

Identifier Source: org_study_id