EUCTR2016-003684-19-DE进行中（未招募）1 期
Xenon-anesthesia on patients undergoing major liver-resection: randomized controlled trial - Xe-Liv
RWTH Aachen, represented by the Rector, himself represented by the Dean of the Medical Faculty0 个研究点目标入组 74 人开始时间: 2017年11月27日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 74
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1.= 3 segment resection
- •2.= 18 years
- •3.Both gender
- •4.ASA I-III
- •5.Written informed consent prior to study participation
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 74
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 74
排除标准
- •1.Severe pulmonary or airway disease
- •2.Severe liver disease, accompanied by a Child–Pugh class >A
- •3.Allergy/hypersensitivity to study medications
- •4.ASA > III
- •5.Patients susceptible to malignant hyperthermia
- •6.Women who are pregnant, breast-feeding or women of childbearing potential not using adequate contraceptive methods
- •7.Patients with elevated intracranial pressure
- •8.Patients legally unable to give written informed consent.
- •9.Patients with preeclampsia or eclampsia
- •10.Patients with a risk of high oxygen demand
- •11.Patients with seriously impaired cardiac function
- •12.All contraindications for xenon anesthesia according to the summary of product characteristics LENOXe
- •13. Patient participates in a parallel interventional clinical trial during this study or receives an investigational drug within 30 days prior to inclusion into this study
研究者
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