跳至主要内容
临床试验/NCT01295398
NCT01295398Unknown不适用

Influence of the Nebulizer on the Clinical Efficacy of Hypertonic Saline 3% in Children Aged Less Than 18 Months and Hospitalized With Acute Viral Bronchiolitis

Assistance Publique Hopitaux De Marseille2 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2010年12月最近更新:
适应症

试验速览

阶段
不适用
入组人数
168
试验地点
2
主要终点
the improvement of the clinical score of severity at the 48th hour between the 3 groups of children

研究概览

简要总结

The aim of the investigators study is to compare in children aged less than 18 months and hospitalized for an acute viral bronchiolitis the efficacy of the HS 3% (Mucoclear®, sterile ampoules of 4 ml) nebulised with a conventional jet-nebulizer (particles diameter of 4-5 µm), or with a jet-nebulizer adapted for infants (particles diameter of 2-2.5 µm), or with a mesh-nebulizer adapted for infants (particles diameter of 2-2.5 µm).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
28 Days 至 18 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Infant of less than 18 months old
  • infant hospitalized for a 1st episode of bronchiolitis defined as a 1st episode of respiratory difficulty with sibilant and\or crépitants in a viral context (head cold and\or cough and\or fever and\or notion of contage)
  • Necessity of an clinical score upper to
  • This clinical score, described by Wang in 1992, is the clinical score classically used in the studies concerning the acute(sharp) bronchiolitis of the infant ( 8,9,12 ). He(it) is at most on 12 points.
  • absence of respiratory décompensation requiring an admission in Unity of Pediatric Intensive care
  • signature of the Informed consent
  • Membership in a national insurance

排除标准

  • Refusal of the parents to participate in the study
  • 18-month-old infant hospitalized for acute(sharp) bronchiolitis with a clinical score lower than
  • signs of respiratory décompensation requiring a transfer in resuscitation, signs of hypercapnie or episodes of apneas
  • histories of bronchiolitis or asthma of the infant
  • cardiac underlying pathology, respiratory, neuromuscular, immunodeficient or former premature of less of 34 weeks of amenorrhoea and less than 3 months of corrected age.
  • child having set within 6 hours preceding the inclusion a treatment by bronchodilatateurs or corticoids by systematic or inhaled way.

结局指标

主要结局

the improvement of the clinical score of severity at the 48th hour between the 3 groups of children

时间窗: 12 months

次要结局

  • tolerance of the nebulisations(12 months)
  • the number of children requiring oxygen(12 months)
  • the number of complications.(12 months)
  • the number of parenteral nutrition(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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