NL-OMON44988已完成不适用
Investigating normal variability in brain volumes and cognition in a healthy population. - Normal variability in brain volumes and cognition
niversitair Medisch Centrum Utrecht0 个研究点目标入组 100 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
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •1) Age between 18 and 70 years
- •2) Written informed consent is obtained
- •3) Female subjects with child-bearing potential need to utilize a proper method of contraception (the pill, vaginal ring, hormonal patch, intrauterine device, cervical cape, condom, contraceptive injection, diaphragm) in case of sexual during the study
排除标准
- •1) MRI contra-indications, e.g.
- •i. Ferrous objects in or around the body (e.g. braces, glasses, pacemaker, metal fragments)
- •ii. Claustrophobia
- •2) Family history with psychiatric illness (i.e. participants themselves, parents, brothers or sisters of the participant
- •3) Chronic use of glucocorticosteroids (temporary use is permitted, if stopped at least 1 month before start of the study)
- •4) Chronic use of non-steroidal anti-inflammatory drugs
- •5) Current use of statins or other lipid-lowering drugs
- •6) Pregnancy or breast-feeding (urine pregnancy test will be performed for sexually active females with child bearing potential)
- •7) Presence of diabetes mellitus, severe heart failure, severe osteoporosis or systemic fungal infections as reported by the participant
- •8) Concurrent use of certain types of medication:
- •i. liver enzyme inducing medication such as carbamazepine, riphampicine, primidone,
- •barbiturates and phenytoine
- •ii. HAART (both HIV protease inhibitors and (non)-nucleoside reverse transcriptase
- •inhibitors), especially efavirenz, ritonavir and lopinavir.
- •iii. telaprevir and boceprevir in treatment of Hepatitis C
研究者
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