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临床试验/NCT01660867
NCT01660867撤回4 期

Nebulized 3% Hypertonic Saline in the Treatment of Acute Bronchiolitis in the Emergency Department

Seoul National University Hospital1 个研究点 分布在 1 个国家开始时间: 2012年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
撤回
试验地点
1
主要终点
hospital admission within 7 days after the day of enrollment

研究概览

简要总结

This is a prospective, randomized, controlled, double-blinded, clinical trial

Subject : 3mo ~ 24mo. aged infants with bronchiolitis

The effect of 3 % NaCl nebulizer or dexamethasone on admission rate of these infants in ED.

详细描述

Randomly assigned to one of three groups

  • Group I : nebulized epinephrine + 0.9% saline + placebo
  • Group II : nebulized epinephrine + 3% saline + placebo
  • Group III : nebulized epinephrine + 0.9% saline + dexamethasone

Group I received two treatments of nebulized epinephrine mixed 0.9% saline and a total of six oral doses of placebo, group II received nebulized epinephrine mixed 3% saline and oral placebo, and group III received nebulized epinephrine mixed 0.9% saline and oral dexamethasone.

The primary outcome is hospital admission within 7 days after the day of enrollment

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
3 Months 至 24 Months(Child)
性别
All
接受健康志愿者

入选标准

  • 3mo ~ 24mo aged patients with bronchiolitis visit to emergency departments
  • RDAI score 4-15

排除标准

  • < 3mo, > 24mo
  • infants who had received oral or inhaled corticosteroids during the preceding 2 weeks
  • infants with a previous episode of wheezing or a diagnosis of asthma
  • any chronic cardiopulmonary disease
  • immunodeficiency
  • infants needed intubation
  • infants with a previous history of apnea or intubation
  • infants with side effect of dexamethasone
  • infants born at less than 37 weeks of gestation who had a corrected age of less than 6 weeks at presentation

研究组 & 干预措施

0.9% saline + oral placebo

Placebo Comparator

nebulized epinephrine + 0.9% saline + placebo => epinephrine + 0.9% saline

干预措施: 0.9% saline + oral dexamethasone (Drug)

3% saline + oral placebo

Experimental

nebulized epinephrine + 3% saline + placebo => nebulized epinephrine + 3% saline

干预措施: 3% saline + oral placebo (Drug)

0.9% saline + oral dexamethasone

Active Comparator

nebulized epinephrine + 0.9% saline + dexamethasone => nebulized epinephrine + 0.9% saline

干预措施: 0.9% saline + oral dexamethasone (Drug)

结局指标

主要结局

hospital admission within 7 days after the day of enrollment

时间窗: within 7 days

hospital admission within 7 days after the day of enrollment(the initial visit to the emergency department)

次要结局

  • Heart rate(baseline, between nebulizer, 60min, 120min, 180min, 240min)
  • RDAI score(baseline, between nebulizer, 60min, 120min, 180min, 240min)
  • respiratory rate(baseline, between nebulizer, 60min, 120min, 180min, 240min)
  • Oxygen saturation(baseline, between nebulizer, 60min, 120min, 180min, 240min)
  • unplanned revisit and admission rate after revisit(in 7days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jin Hee Lee

Assistant Professor

Seoul National University Hospital

研究点 (1)

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