ACTRN12608000098336尚未招募未知
A comparison of oral and intravenous saline to replace ileostomy fluid losses in infants (pilot study)
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 10
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
- Open (masking not used)
入排标准
- 年龄范围
- 14 Days 至 6 Months（—）
- 性别
- All
入选标准
- •Infants with an ileostomy will be considered eligible for inclusion if:
- •They are stable on full enteral feeds, or within 48 hours of ceasing total parenteral nutrition (TPN).
- •They require replacement fluid for ileostomy losses between 20 – 40 mL/kg/day.
- •They are already receiving additional salt supplementation as part of clinical care.
- •Signed, informed parental consent can be obtained prior to enrollment.
- •The treating Consultant Neonatologist gives permission for enrollment.
- •All gestational age, birth weight, weight at enrollment, and surgical diagnoses will be eligible.
排除标准
- •Infants with an ileostomy will be excluded if they have:
- •Ileostomy loss >40ml/kg/day.
- •A known chronic salt losing condition, such as renal failure or congenital adrenal hyperplasia.
- •Requirement of mechanical ventilation support via an endotracheal tube.
- •Haemodynamic instability despite maximal inotropic and fluid support.
研究者
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