EUCTR2014-005472-29-IT进行中（未招募）1 期
Safety and efficay of 0.2% propranolol eye drops in newborns with retinopathy of prematurity: a pilot study - na
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 96
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. Newborns with gestational ages between 23 and 32 weeks affected by classic stage 1 ROP.
- •2. Parents informed consent.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •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
- •Newborns with:
- •1. cardiac failure
- •2. recurrent episodes of bradycardia (BPM < 90)
- •3. atrioventricular block 2nd and/or 3rd degrees
- •4. significant cardiovascular congenital anomalies (except of patent foramen ovale, patent ductus arteriosus o defects of the interventricular septum)
- •5. hypotension
- •6. serious renal failure
- •7. cerebral bleeding (ongoing)
- •8. other diseases for which the use of beta blockers is contraindicated
- •9. ROP stage > 1
研究者
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