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临床试验/EUCTR2015-001077-40-SE
EUCTR2015-001077-40-SE进行中(未招募)1 期

INNOVATIVE STEROID TREATMENT TO REDUCE ASTHMA DEVELOPMENT IN CHILDREN AFTER FIRST-TIME RHINOVIRUS INDUCED WHEEZING – THE INSTAR STUDY - INSTAR

St. Olavs Hospital0 个研究点目标入组 280 人开始时间: 2019年12月6日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
280

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • 1.age 3-24 months,
  • 2.first acute severe wheezing episode, defined as first-time acute breathing difficulty with wheezing ever, appearing less than 7 days from onset of symptoms, in a child admitted to hospital, and with one or more of
  • -hypoxia (SAT O2 = 92%)
  • -retractions (inter-, subcostal),
  • -prolonged expiration (on auscultation),
  • -expiratory rhonchi (on auscultation)
  • 3.rhinovirus positive PCR test in nasopharyngeal secrete,
  • 4.signed informed consent and expected cooperation of the patients for the treatment and follow up must be obtained and documented according to ICH GCP, and national/local regulations.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 280
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.previous episodes with wheezing, defined as a history of acute breathing difficulty with wheezing in need of treatment at a general practitioner or at hospital, or parental information about similar breathing difficulties
  • 2.gestational age <37 weeks
  • 3.chronic illness other than atopy (eczema),
  • 4.previous systemic or inhaled corticosteroid treatment,
  • 5.participation to another trial,
  • 6.varicella infection or contact during the last 2-3 weeks,
  • 7.need for intensive care unit treatment during the present infection, except for respiratory support with high flow nasal cannula ventilation,
  • 8.any reason why, in the opinion of the investigator, the patient should not participate (e.g. not able to comply with study procedures).

研究者

发起方
St. Olavs Hospital

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