跳至主要内容
临床试验/NL-OMON35544
NL-OMON35544招募中不适用

Memory formation under stress in humans - the importance of the Mineralocorticoid Receptor - Memory & the MR

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 96 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
招募中
发起方
入组人数
96

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 99(—)

入选标准

  • - Male, healthy volunteers
  • - Age 18 - 35 years
  • - Normal or corrected-to-normal vision
  • - Normal uncorrected hearing
  • - Body mass index between 18.5 and 30
  • - Willingness and ability to give written informed consent and willingness and ability to understand the nature and content, to participate and to comply with the study requirements

排除标准

  • - Acute or history of renal insufficiency / impairment of renal excretory function (or creatinine levels > 1.1 mg/dl at screening)
  • - Hyperkalemia (or potassium levels of > 5.0 mEq/L at screening)
  • - History of psychiatric treatment /current psychiatric treatment
  • - History of neurological treatment /current neurological treatment
  • - History of endocrine treatment /current endocrine treatment
  • - History of autonomic failure (e.g., vasovagal reflex syncope)
  • - History of psychotropic medication (e.g. antidepressants)
  • - History of hepatic impairments
  • - History of cardiovascular diseases
  • - Hypotension (< 90 / 60 mmHG)
  • - Bradycardia / Tachycardia (heart rate < 50 or > 100 at rest)
  • - Use of any medication on a regular basis
  • - Metal objects in or around the body
  • - Irregular sleep/wake rhythm (e.g., regular nightshifts or cross timeline travel)
  • - Claustrophobia
  • - Use of recreational drugs weekly or more often
  • - Smoking of more than 5 cigarettes per day
  • - Average use of more than 3 alcoholic beverages daily and self-reported inability or un-ease to cease drinking alcohol for 24 hours prior to testing.
  • - Caffeine consumption 3 hours before testing
  • - Professional sports or participation in competitions (as Spironolacton can lead to a positive doping test)

研究者

发起方
niversitair Medisch Centrum Sint Radboud

相似试验