EUCTR2013-002062-39-IT进行中（未招募）不适用
Safety and efficacy of propranolol eye drops in neonates with retinopathy of prematurity: a pilot study (DROP-ROP). - DROP-ROP trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
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
- •Preterm newborns (gestational age lower than 32 weeks) who develop stage 2 ROP (zone II without plus).
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 55
- •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. Newborns with heart failure, bradycardia, atrioventricular blocks, congenital cardiovascular anomalies, hypotension, renal failure, failure to thrive, cerebral haemorrhage, other diseases that contraindicate the use of beta-blockers.
- •2. Newborns with ROP at a more advanced stage than stage 2 (zone II without plus).
研究者
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Safety and Efficacy of Propranolol in Newborns With Retinopathy of Prematurity (PROP-ROP)Retinopathy of prematurity (ROP), the leading cause of blindness in childrenNeonatal DiseasesOther retinal disordersISRCTN18523491A. Meyer University Children's Hospital (Italy)44