ITMCTR2100004871已完成4 期
The efficacy, safety and quality of life of tandospirone and shuganjieyu capsule in the treatment of comorbid anxiety and depression of epilepsy
试验速览
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 18 至 75（—）
- 性别
- All
入选标准
- •1. Aged 18 to 70 years;
- •2. The clinical manifestations and EEG changes of the patients were in line with the 2017 epilepsy diagnostic criteria formulated by the International Anti-Epilepsy Union (ILAE), and epilepsy was classified;
- •3. Antiepileptic drugs remained unchanged in the two groups;
- •4. According to the relevant diagnostic points of depression and anxiety in the 10th edition of the International Classification of Diseases (ICD-10), one professional neurologist and one psychiatrist respectively completed the relevant scale, with CNDDIE score of > 12 points and GAD-7 score of > 6 points.
排除标准
- •1. Epileptic status or non-epileptic seizure;
- •2. Patients with severe depression or suicidal tendencies;
- •3. Previous depression and anxiety, history and family history of mental illness, severe mental illness or being under treatment;
- •4. Pregnant or lactating women;
- •5. Patients who have taken anti-depressant and anxiety-related drugs or are allergic to the two intervention drugs used in this study within the last 2 weeks.
研究者
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