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
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