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临床试验/NCT00496574
NCT00496574Unknown4 期

Evaluation of Long-term Clinical Efficacy of House Dust Mite Immunotherapy in Children With Bronchial Asthma

Medical University of Lodz2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2006年5月最近更新:
适应症

试验速览

阶段
4 期
入组人数
60
试验地点
2
主要终点
clinical symptoms, reliever drugs usage, inhaled glucocorticosteroid usage, quality of life, lung function

研究概览

简要总结

The aim of the study is to assess the effect of specific immunotherapy (SIT) to dust mites on clinical symptoms, reliever drugs usage, inhaled glucocorticosteroid usage, quality of life, lung function, bronchial hyperreactivity with methacholine, and presence and type of allergy after three years of SIT in children with asthma.

详细描述

According to Global Initiative for Asthma treatment of asthma is based on avoidance of allergens, pharmacological treatment, and specific immunotherapy.

The aim of the study is to assess the effect of specific immunotherapy (SIT) to dust mites on clinical symptoms, reliever drugs usage, inhaled glucocorticosteroid usage, quality of life, lung function, bronchial hyperreactivity with methacholine, and presence and type of allergy after three years of SIT in children with asthma.

研究设计

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

入排标准

年龄范围
8 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • patients allergic to house dust mites
  • patients with moderate bronchial asthma
  • patients with controlled asthma
  • patients who were qualified for immunotherapy and gave written informed consent for immunotherapy (active treatment group)
  • patients who were qualified for immunotherapy and did not agree with this kind of treatment - did not give written informed consent for immunotherapy (control group)

排除标准

  • patients allergic for other perennial and seasonal allergens
  • patients with other chronic diseases that either put the patient at risk when participating in the study or could influence the results of the study or the patient's ability to participate in the study as judged by the investigator
  • medications that resulted in patient exclusion included:anti-parasites or oral corticosteroids within 6 months before the first visit.

结局指标

主要结局

clinical symptoms, reliever drugs usage, inhaled glucocorticosteroid usage, quality of life, lung function

时间窗: baseline (first visit), 12 months (second visit), 24 months (third visit), 36 months (fourth visit)

次要结局

  • bronchial hyperreactivity with methacholine, and presence and type of allergy after tree years of SIT in children with asthma.(after 36 months (fourth visit))

研究者

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

Iwona Stelmach

MD, PhD, Professor

Medical University of Lodz

研究点 (2)

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