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临床试验/IRCT2014122610279N4
IRCT2014122610279N4已完成3 期

Comparing the effect of repeated low dose and unique high dose sucrose with placebo (distilled water) on the control of pain secondary to retinopathy of prematurity examination of premature neonates

Ministry of Health of Turkey, General Directorate of Pharmaceuticals and Pharmacy0 个研究点目标入组 64 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
64

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
28 days 至 2 months(—)
性别
All

入选标准

  • Inclusion criteria;
  • 1. Premature neonates who underwent first retinopathy of prematurity examination
  • Exclusion criteria;
  • 1. Invasive or noninvasive mechanical ventilation therapy during retinopathy of prematurity examination.
  • 2. Neonates who take analgesia, sedative medicine.
  • 3. Asphyxia
  • 4. Intraventricular hemorrhage
  • 5. Neonates who were resuscitated
  • 6. Neonates who had congenital anomaly

排除标准

  • 未提供

研究者

发起方
Ministry of Health of Turkey, General Directorate of Pharmaceuticals and Pharmacy

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