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临床试验/NCT02950974
NCT02950974已完成不适用

Change in Serum Chloride Level After Loading Dose of Sterofundin Solution Compared With Normal Saline Solution

Ramathibodi Hospital0 个研究点目标入组 20 人开始时间: 2014年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
20
主要终点
Change in serum chloride

研究概览

简要总结

Prospective, crossover, randomized trial to evaluate plasma compositions after loading dose of sterofundin solution given to healthy volunteer in the resuscitation manner compared with normal saline solution.

详细描述

10 healthy volunteers were randomly assigned to receive either normal saline or sterofundin for the first solution in dose of 30 mL/kg (max 2 L) over 1 hour. Blood was collected at baseline (T0), at 60 minutes (T1), 120 minutes (T2), and 240 minutes (T4) from baseline. Time to fist void after initiation of fluid and urine volume were also recorded. After wash-out period of at least 1 week, crossover studies were performed with another fluid.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (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

入选标准

  • No underlying disease
  • LVEF > 0.5
  • No current medication usage

排除标准

  • Pregnancy or lactation
  • BMI <18 or >25
  • Fever presented in the past 2 weeks

研究组 & 干预措施

NSS

Active Comparator

NSS 30 ml/kg (maximum of 2 litres) intravenous load over 1 hour

干预措施: Sterofundin (Drug)

NSS

Active Comparator

NSS 30 ml/kg (maximum of 2 litres) intravenous load over 1 hour

干预措施: NSS (Drug)

Sterofundin

Experimental

Sterofundin solution 30 ml/kg (maximum of 2 litres) intravenous load over 1 hour

干预措施: Sterofundin (Drug)

Sterofundin

Experimental

Sterofundin solution 30 ml/kg (maximum of 2 litres) intravenous load over 1 hour

干预措施: NSS (Drug)

结局指标

主要结局

Change in serum chloride

时间窗: 4 hours

At 0, 1, 2, and 4 hours from initiation

次要结局

  • Change in serum pH(4 hours)
  • Change in serum osmolality(4 hours)
  • Change in serum SID(4 hours)
  • Time to first void(Within 24 hours)
  • Urine volume(Within 24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Cherdkiat karnjanarachata

Dr.

Ramathibodi Hospital

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