跳至主要内容
临床试验/NL-OMON44988
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

发起方
niversitair Medisch Centrum Utrecht

相似试验