临床试验/NCT02776020

NCT02776020Unknown不适用

Non-invasive, Real-time Anesthetic Drug-monitoring System

Rambam Health Care Campus0 个研究点目标入组 30 人开始时间: 2016年6月最近更新: 2016年5月18日

适应症

试验速览

阶段: 不适用
发起方: Rambam Health Care Campus
入组人数: 30
主要终点: Changes in Propofol Blood Levels

研究概览研究设计入排标准结局指标研究者记录与标识符相似试验

研究概览

简要总结

The aim of this study is to determine efficacy of the "CorrecDose" device to continuously and non-invasively follow the changes in propofol concentrations in the participants' blood.

研究设计

研究类型: Observational
观察模型: Case Only
时间视角: Prospective

入排标准

年龄范围: 18 Years 至 50 Years（Adult）
性别: Female
接受健康志愿者: 是

入选标准

•Women who have signed Informed consent form
•Women undergoing Trans vaginal ovum retrieval (TVOR) for invitro fertilization (IVF) and will be sedated with propofol administered intravenos (IV)

排除标准

•Women with background diseases
•Women with chronic use of drug and medication
•Women with peripheral blood vessels problems
•Women with high blood pressure
•Women with body mass index (BMI) score over 35 or less than 18

结局指标

主要结局

Changes in Propofol Blood Levels

时间窗: Half hour

Graphic display on monitor of real-time changes

次要结局

未报告次要终点

研究者

发起方

Rambam Health Care Campus

申办方类型

Other

责任方

Principal Investigator

主要研究者

ABECASSIS PHILIPPE

Head of women and obstetrics anesthesiology unit

Rambam Health Care Campus

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