NL-OMON53199已完成不适用
The feasibility of using a subtherapeutic dose of piracetam as a marker of adherence to therapy - Subtherapeutic dose of piracetam as a therapy adherence marker
ederlands Kanker Instituut0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 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
- 18 至 64（—）
入选标准
- •To be considered eligible to participate in this study, all of the following
- •requirements must be
- •1. Age >= 18 years;
- •2. Able and willing to give written informed consent;
- •3. Able and willing to undergo urine sampling for analysis;
- •4. Able and willing to digest multiple tablets at day one of each study week (6
- •1.25 mg in week 1; 4 tablets of 1.25 mg in week 2; 2 tablets of 1.25 mg in week
- •3 and 1 tablet of 1.25 mg in week 4)
排除标准
- •A potential subject who meets any of the following criteria will be excluded
- •from participation in this study:
- •1. Current prescribed treatment with piracetam;
- •2. Pregnant or breastfeeding;
- •3. Criteria regarding the following contra-indications for piracetam:
- •- Cerebral haemorrhage;
- •- Huntington's chorea;
- •- Hypersensitivity to pyrrolide derivatives.
研究者
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