DRKS00032532招募中不适用
Prospective, multi-centre, non-interventional study on the use, tolerability and safety of the One Strength dose escalation scheme with NOVo Helisen® hoUSe dust mites in everyday practice - NOVUS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 1,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 12 Years 至 one(—)
- 性别
- All
入选标准
- •1. Written informed consent from the patient. In the case of patients under the age of 18, the consent of both parents/legal guardians is also required.
- •2. Patients treatment with the One-Strength dose escalation scheme of NH (D.p./D.f.) must be approved, in accordance with the specifications of the SmPC. This includes adolescents (=12 and <18 years) and adults with allergic (IgE-mediated) diseases such as allergic rhinitis, allergic conjunctivitis, allergic bronchial asthma (see section 4 of the current SmPC).
- •3. The therapy decision must precede the decision to participate in the study and must be independent.
排除标准
- •1. Any contraindication according to section 4.3 of the current SmPC for NH (D.p./D.f.) for the One-Strength dose escalation scheme.
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