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临床试验/CTIS2024-512438-14-00
CTIS2024-512438-14-00进行中(未招募)1 期

Klonidin as pain relief in eye examination of premature infants - cloROP

Region Oerebro Laen0 个研究点目标入组 50 人开始时间: 2024年7月8日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 17(—)
性别
All

入选标准

  • The infant is admitted to the study clinic, The infants guardian/s has/have given their written consent to the child's participation in the study, The infant is born before gestation week 30

排除标准

  • Children who has received beta blockers, pain reliever or sedating drug within 24 hours of eye examination., Previously documented kidney failure, Does not have a gastric tube, Neurologically affected, Known cardiac arrhythmia, Circulatory instability (defined as mean arterial pressure lower than the child's gestational age)

研究者

发起方
Region Oerebro Laen

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