DRKS00033174已完成不适用
se of bioreactance technology for early detection of reduced stroke volume during cesarean delivery under spinal anesthesia
niversitätsklinikum Marburg0 个研究点目标入组 60 人开始时间: 2023年12月6日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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
- Female
入选标准
- •Patients undergoing an elective caesarean delivery
- •- Spinal anaesthesia as an anaesthesia procedure for caesarean delivery
- •- Signed informed consent for inclusion in this study
排除标准
- •- Patients < 18 years of age
- •- No SPA, but primarily general anaesthesia as the anaesthetic procedure for the caesarean section
- •- Patients who do not wish to participate in the examination (i.e. there is no signed consent form)
- •- Patients in whom the placement of the four adhesive electrodes is not possible for medical reasons (e.g. extensive wound or skin rash in the target area)
- •- Contraindications according to the manufacturer of the Starling monitor (Baxter)
- •- Presence of severe (clinically relevant) aortic valve insufficiency
- •- Severe anatomical anomalies of the thoracic aorta, e.g. (large) synthetic aortic grafts
- •- external / internal pacemakers with unipolar electrodes
研究者
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