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临床试验/NL-OMON30665
NL-OMON30665已完成3 期

Twin SUBLIVAC® Grasses Clinical Efficay Study - niet van toepassing

HAL Allergenen Lab0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
12 至 99(—)

入选标准

  • Subjects with allergic rhinoconjunctivitis with or without mild asthma (FEV1 >= 70%) for at least 2 years. Their allergic symptoms should be related to grass pollen
  • Use of anti-allergy symptomatic medication in the last pollen season (or, in case of a low pollen season, in one of the two previous years)
  • A positive skin prick test (>3 mm) for grasses and specific serum IgE-test
  • (>1 U/ml) for grass pollen (Lolium perenne, Phleum pratense and Poa pratensis).
  • Age 12 years or older.
  • Subjects (and their parents if required) shall give a written informed consent

排除标准

  • A positive SPT for perennial allergens of house dust mite
  • Symptoms related to concomitant sensitisation to perennial allergens of pets
  • Chronic asthma or emphysema, particularly with a FEV1 < 70 % of predicted value or use of inhalation corticosteroids outside grass and tree pollen season for more than two episodes and/or longer than fourteen days
  • Use of symptomatic medication for more than three episodes and/or longer than three days outside the tree- or grasspollen season
  • Serious immuno-pathological diseases or malignancies (including auto-immune diseases, tuberculosis, HIV)
  • Inflammation and infection of the target organ
  • Severe atopic dermatitis requiring systemic immuno-suppressive medication
  • Allergen specific immuno-therapy treatment within the last 5 years for a period longer than three months

研究者

发起方
HAL Allergenen Lab

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