跳至主要内容
临床试验/EUCTR2008-002277-13-DE
EUCTR2008-002277-13-DE进行中(未招募)不适用

Double blind, randomized, placebo-controlled clinical trial to proof the efficacy and tolerability of the homeopathic medicinal product Klosterfrau Allergin Globuli in comparison to placebo in children at the age of 6-11 years with hey fever

MCM Klosterfrau Vertriebs GmbH0 个研究点开始时间: 2009年1月30日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

性别
All

入选标准

  • 6 - 11 years of age
  • clinically diagnosed hay fever
  • At least 4 of the following symptoms (total sum score of at least 8 points): itchy nose, runny nose, blocked nose, sneezing, red eyes, itchy eyes, tearing
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 260
  • 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

  • Sensitivity to components of the IMP
  • Severe diseases of the respiratory tract (e. g. Asthma bronchiale, chronic bronchial obstruction) as well as other severe organ diseases
  • Intolerability to sacchrose
  • Intake of cromones
  • Intake or topical application of antihistaminics
  • Intake or topical application of glucocorticoids
  • Nasal sympathomimetics
  • Atopic dermatitis (medium to severe grade)
  • Patients with food allergy
  • Person who is committed to a facility (home, psychiatric clinic)
  • Respiratory diseases requiring glucocorticoids
  • Heritable fructose intolerance
  • Specific immune therapy or change of antigen dose within the previous month

研究者

发起方
MCM Klosterfrau Vertriebs GmbH

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