EUCTR2015-000486-31-EE进行中（未招募）不适用
The effect of milrinone on central and regional blood flow in preterm neonates undergoing patent ductus arteriosus ligation.
Department of Anaesthesiology and Intensive Care, University of Tartu0 个研究点开始时间: 2015年5月19日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1)Neonates and infants up to 90 days of age
- •2)Haemodynamically significant PDA requiring surgical ligation
- •3)Arterial catheter and/or central venous catheter in place on clinical indication
- •4)Informed consent given by the parents or guardians
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 30
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1)Renal failure requiring renal replacement therapy (peritoneal dialysis) or serum creatinine >100 µmol/l or oliguria <0.5 ml/kg/min within 6 hours
- •2)Hypersensitivity to milrinone or any other component of the study drug
- •3)Situation where the treating physician considers milrinone to be contraindicated
- •4)Major congenital malformation
- •5)Known metabolic disease
- •6)Informed consent from parents or guardians not obtained
- •7)Critically unstable state of the patient, likely fatal within 72 hours
- •8)The patient is already recruited in another clinical trial investigating a medical product
研究者
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