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临床试验/NL-OMON54413
NL-OMON54413已完成不适用

PJ-008200 Measurements on healthy subjects to design a nociception index - Measurements to design a nociception index

Philips Patient Monitoring (Philips Medizin-Systeme Böblingen GmbH)0 个研究点目标入组 40 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
40

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 64(—)

入选标准

  • 1) Age between 18 and 65 years old
  • 2) ASA I Healthy subjects
  • 3) BMI < 35
  • 4) Females should be using contraception

排除标准

  • 1) Pregnancy (pregnancy test before start protocol, if female, with the
  • exception of post menstrual women)
  • 2) Smoking
  • 3) Alcohol abuse
  • 4) Medication that influeunces the central or peripheral nervous system, or the
  • cardiovascular system
  • 5) Drug use (drug test before start protocol)
  • 6) Raynaud's disease (poor blood circulation)
  • 7) Scleroderma, Dupuytren*s Contracture, or other Rheumatology issues
  • 8) Depression and/or anxiety (the Hospital Anxiety and Depression Scale (HADS)
  • questionnaire is given before the start of the protocol. Subjects with a score
  • greater than or equal to 11 are excluded)
  • 9) Food eaten in the 6 hours before the test
  • 10) Fluid intake within less than 2 hours of the planned start of
  • experimentation
  • 11) Use of caffeinated beverages in the 12 hours before the test
  • 12) Use of caffeinated food (e.g. chocolate) in the 6 hours before the test
  • COVID-19 additional
  • 13) Currently displaying COVID-19-related symptoms, namely a fever, cough
  • and/or difficulty breathing
  • 14) Having been positively tested as infected with COVID-19 in the past 14 days
  • 15) Travelled to or from high risk COVID-19 areas in the past 14 days
  • 16) Been in contact with a (suspected) COVID-infected person in the past 14

研究者

发起方
Philips Patient Monitoring (Philips Medizin-Systeme Böblingen GmbH)

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