EUCTR2021-004548-64-PL进行中(未招募)1 期
Multicenter, randomized, double-blind, placebo controlled study to assess the efficacy and safety of Rapamycin in drug Resistant Epilepsy associated with TSC (RaRE-TS) - RaRE-TS
The Children's Memorial Health Institute0 个研究点目标入组 200 人开始时间: 2022年12月8日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •-male or female aged from 3 months up to 50 years at the day of randomization
- •-patients/parents/caregivers are willing to and able to give informed consent form for the participation in the study
- •-patients/parents/caregivers are willing to and able to comply with all study requirements
- •-definite diagnosis of TSC according to the Consensus criteria (Northrup, 2013)
- •-drug-resistant epilepsy associated with TSC with at least 8 seizures during 4 weeks
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 160
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 40
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-history of treatment with mTOR inhibitor in the three months prior to screening,
- •-history of pseudo-epileptic seizures,
- •-history of progressive CNS disease other than TSC
- •-recent surgery within 2 weeks prior to the screening
- •-severe infection within 2 weeks prior to the screening
- •-use of the cannabis derivatives
- •-contraindications for MRI or general anesthesia
- •-occurrence of the serious comorbidities which, in the opinion of the investigator, may either put a patient at significant risk associated with the
- •participation in the study or may influence the results of the study the investigator
- •-pregnancy
研究者
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