ACTRN12621000721808招募中未知
Effect of Vasopressor Infusion via Peripheral vs Central Access on 60 day survival in patients with shock - (The VIPCA trial)
Caboolture Hospital0 个研究点目标入组 40 人开始时间: 2021年6月9日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •* Patients admitted to Caboolture Hospital ED
- •* Any unplanned admission to Caboolture Hospital ICU
- •* greater than 18 years
- •* Treating clinician has deemed that a Vasopressor Infusion is required
排除标准
- •* Pregnancy or suspected pregnancy
- •* Treating clinician believes that survival beyond 48 hours is unlikely or patient being admitted to ICU solely for Palliation or Organ Donation
- •* Has received vasopressor infusion for 4 hours
- •* Requiring >0.1mcg/kg/min noradrenaline (or equivalent dose of other vasopressors) at the time of screening; or requiring >1 vasopressor agent
- •* Patient already has a CVC in-situ or requires a CVC insertion for specific therapies other than vasopressors (e.g., total parenteral nutrition, severe electrolyte derangements like: K+ less than or equal to 2.0 mmol/L, PO4-2 less than or equal to 0.3 mmol/L, or for Ca+2 infusion for CRRT)
研究者
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