JPRN-UMIN000006398已完成2 期
Clinical pharmacological trial of TM8001 for schizophrenia associated with carbonyl stress - Clinical pharmacological trial of TM8001 for schizophrenia associated with carbonyl stress
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 65years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •creatinin >2mg/dL or BUN > 25mg/dL. HbA1c > 6.1% and fetal blood suger > 126mg/dL or blood suger > 200mg/dL. AST, ALT over 2.5 fold of standard level. Total bilirubin > 3mg/dL. sever cardiac diseases, lung diseases, hepatic diseases, neurological diseases, hematological diseases, endocrine diseases,immune diseases, other sever diseases. History of anaphylaxis shock, drug allergy. History of taking aminophylline , teophylline, cholinteophylline, levodopa within 4 weeks before trail. History of taking ECT within 3 months before trail. Possible risk of suicide. History of cancer within 5 years before trail. Participating other trial. Pregnancy. Inappropriate regarded by the responsible doctor.
研究者
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