跳至主要内容
临床试验/NL-OMON49452
NL-OMON49452尚未招募不适用

Optimisation of research protocols for respiratory challenges with the RespirAct (RA-MR)TM in healthy volunteers - RespirAct

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
80

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

  • - Signed informed consent
  • - Age: 18-90 years
  • - Healthy subject (defined as a volunteer who is not referred to Erasmus MC
  • with signs and symptoms of disease)

排除标准

  • - No informed consent
  • - Subjects refusing to undergo testing
  • - Subjects with obstructive or resistive lung disease whose PaCO2 at rest is
  • greater than 50mmHg or whose venous serum bicarbonate is greater than 26 mEq/L
  • - Subjects with pre-existing respiratory acidosis
  • - Subjects who require portable oxygen at rest or with exercise
  • - Subjects with chronic heart failure or severe pulmonary disease who are
  • unable to climb one flight of stairs due to shortness of breath
  • - Subjects with severe heart failure or restrictive lung disease with resting
  • respiratory rate over 15 breaths/min
  • - Subjects with a typical contra-indication to an MRI exam
  • - Subjects with metal implants
  • - Woman who are pregnant or lactating
  • - Having any physical or mental status that interferes with the informed
  • consent procedure

研究者

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