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临床试验/DRKS00014788
DRKS00014788尚未招募不适用

Validation of a Propofol Detector (EDMON) for Anesthesia during a Single Lung Ventilation (SLV) Surgery - EDMON-ELV

Center of Breath Research Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie Universitätsklinikum des Saarlandes0 个研究点目标入组 30 人开始时间: 2018年6月4日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30

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 Years 至 one(—)
性别
All

入选标准

  • Written consent of the patient; Patients undergoing elective surgery for general anesthesia who require single-lung ventilation for surgical reasons; an arterial cannula is required for the procedure and / or postoperative care; Age = 18 years; ASA I-III; No significant hepatic, nephrological, neurological and cardiac pre-existing conditions; BMI <35; No participation in another study (up to 30 days before enrollment in the study); In women of childbearing potential: negative pregnancy test, or surgical sterilization or contraceptive use during the examination or min. 2 years after postmenopause

排除标准

  • Contraindications or known intolerance to any of the medicines or procedures used; Pre-existing conditions or patient circumstances that make it impossible or meaningless to examine the patient (for example, dementia, psychiatric disorders, lack of understanding of speech or ability to speak); Patients with significant cardiac pre-existing conditions; Body Mass Index > 35; ASA status> III; drug abuse; Positive HIV or hepatitis test; Pregnancy; Rejection by the patient

研究者

发起方
Center of Breath Research Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie Universitätsklinikum des Saarlandes

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