ISRCTN66987216已完成未知
A randomised, double-blind, placebo-controlled, two-phase study on the impact of Doxycycline on fear memory in healthy individuals
Psychiatric University Hospital (Psychiatrische Universitätsklinik) Zürich (PUK ZH)0 个研究点目标入组 160 人开始时间: 2015年6月23日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 160
研究概览
简要总结
2018 Results article in https://www.ncbi.nlm.nih.gov/pubmed/28373691 results (added 09/07/2019) 2019 Results article in https://pubmed.ncbi.nlm.nih.gov/31615840/ (added 10/07/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Informed consent as documented by signature
- •2. Age 18 – 40 years
排除标准
- •1. Allergy to Doxycycline or to any other ingredient in the named drug
- •2. Use of any drugs in the 2 weeks prior to the study with the exception of contraceptive drugs and incidental use of NSARs or paracetamol
- •3. Women who are pregnant or breast feeding
- •4. Intention to become pregnant during the course of the study
- •5. Lack of safe contraception, defined as: Female participants of childbearing potential, not using and not willing to continue using a medically reliable method of contraception for the entire study duration, such as oral, injectable, or implantable contraceptives, or intrauterine contraceptive devices, combined with a mechanical contraceptive (condom, diaphragm)
- •6. Other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, etc.)
- •7. Any history of psychiatric, neurological, dependence or systemic/rheumatic disease
- •8. Known or suspected non-compliance, drug or alcohol abuse
- •9. Inability to follow the procedures of the study, e.g. due to language problems
- •10. Participation in another study with investigational drug within the 30 days preceding and during the present study
- •11. Previous enrolment into the current study
- •12. Members of the study team and their family members and dependants
研究者
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