NL-OMON49710已完成不适用
Iohexol for measuring renal function. - HERO-study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 125
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 2 至 17（—）
入选标准
- •0-18 years of postnatal age
- •>37 weeks of gestational age (for infants < one year postnatal age)
- •Bodyweight >2500g
- •Patients admitted to pediatric or neonatal intensive care unit
- •PELOD-II (pediatric logistic organ dysfunction score) of 1 or higher (<= at
- •least one failing organ)
- •Indwelling central line or arterial line in place for clinical purposes, or
- •scheduled regular blood work for clinical reasons (at least once a day)
- •Informed written consent
排除标准
- •Known medical history of allergic reaction to injection of iodinated contrast
- •Receiving renal replacement therapy
- •Language or cognitive inability (of parents/caregivers) to understand written
- •and oral informed consent.
研究者
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