Skip to content

Clinical efficacy evaluation of anti epileptic drugs for post-stroke epilepsy

Clinical efficacy evaluation of antiepileptic drugs for post-stroke epilepsy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093722
Enrollment
Unknown
Registered
2024-12-10
Start date
2023-01-02
Completion date
Unknown
Last updated
2024-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post stroke epilepsy

Interventions

Research group:Levetiracetam tablets,The initial dose is 0.5g/time, twice a day, orally administered, and then the dose is adjusted according to the recovery of the condition, increasing to 1.0g/time,
control group:oxcarbazepine tablets,The initial dose is 8-10mg/Kg, taken orally twice a day, and then adjusted according to the recovery of the condition. The maximum daily dose should not exceed 600m

Sponsors

Daizhuang Hospital in Shandong Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
36 Years to 76 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria outlined in the Minutes of the 6th National Conference on Cerebrovascular Disease; 2. Diagnosis of cerebrovascular disease by cranial CT or MR; 3. Complete case data; 4. Both the patient and their relatives were informed and voluntarily joined this trial.

Exclusion criteria

Exclusion criteria: 1. Individuals with combined cognitive impairment, communication disorders, history of primary epilepsy, severe infections, and malignant tumors; 2. History of drug dependence or allergy; 3. Poor compliance and inability to cooperate with treatment.

Design outcomes

Primary

MeasureTime frame
electroencephalogram;

Secondary

MeasureTime frame
Interleukin-2;Interleukin-6;Enolase;Tumor necrosis factor - a;Adverse reactions;

Countries

China

Contacts

Public ContactWang Zhonggang

Daizhuang Hospital in Shandong Province

wzg969@163.com+86 150 2077 8402

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026