临床试验/NCT02880566

NCT02880566Unknown不适用

Efficacy of Scalp Block on Hemodynamic Stability and Opioid Consumption During Craniotomy

University of Liege0 个研究点目标入组 50 人开始时间: 2016年9月最近更新: 2016年8月26日

适应症

试验速览

阶段: 不适用
发起方: University of Liege
入组人数: 50
主要终点: Hemodynamic stability

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

Prospective randomised double-blinded placebo-controlled trial on the efficacy of scalp blocks on hemodynamic stability and opioid consumption during and after craniotomy.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Treatment
盲法: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Elective craniotomy for supratentorial lesion

排除标准

•Allergy to local anaesthetic
•Psychiatric disease
•Inability to consent
•Uncontrolled intracranial hypertension

结局指标

主要结局

Hemodynamic stability

时间窗: 5 minutes

Increased in mean arterial pressure or heart rate of more than 15 % within 5 minutes of head pinning

次要结局

Cumulative intraoperative remifentanil consumption(24 hours)
Postoperative pain scores(48 hours)
Cumulative postoperative morphine consumption(48 hours)

研究者

发起方

University of Liege

申办方类型

Other

责任方

Principal Investigator

主要研究者

Jean François Brichant

Professor and Chair

University of Liege

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