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临床试验/ChiCTR1800016580
ChiCTR1800016580进行中(未招募)诊断试验新技术临床试验

實時超聲波引導脊椎麻醉:評估使用橫向平面超聲波檢查的新技術

Department of Anaesthesia & Intensive Care, CUHK1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 1990年1月1日最近更新:

试验速览

阶段
诊断试验新技术临床试验
状态
进行中(未招募)
发起方
入组人数
30
试验地点
1
主要终点
Feasibility & technical ease of doing spinal anaesthesia under real time ultrasound guided transverse in-plane approach from the dependent side

研究概览

简要总结

評估使用橫向平面超聲波檢查的新技術

研究设计

研究类型
观察性研究
主要目的
单臂
盲法
N/a

入排标准

年龄范围
20 至 85(—)
性别
All

入选标准

  • Patients who are between 20 to 85 years old, of American Society of Anaesthesiology (ASA) physical status classification I-III, and scheduled to undergo elective groin, lower limb, lower abdominal surgical, gynaecological and urogenital procedures under spinal anaesthesia.

排除标准

  • Patient refusal or unwilling to participate, ASA physical status >III, spinal deformity, previous spine surgery, pregnancy, coagulopathy, allergy to local anaesthetic drugs, skin infection at the site of needle insertion, severe cardiac disease such as atrial stenosis, atrial fibrillation, autonomica dysfunction, and sepsis.

研究组 & 干预措施

Case series

Nil

结局指标

主要结局

Feasibility & technical ease of doing spinal anaesthesia under real time ultrasound guided transverse in-plane approach from the dependent side

时间窗: once during spinal anaesthesia

Cerebrospinal fluid (CSF) efflux time

时间窗: once during spinal anesthesia

次要结局

  • Rate of successful attempt, number of spinal needle pass, patient satisfaction score, any intraoperative or postoperative complications in the next 24 hours(within 24 hours after Spinal Anaesthesia)

研究者

发起方
Department of Anaesthesia & Intensive Care, CUHK

研究点 (1)

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