KCT0007260招募中未知
Analysis of the difference in the incidence rate of adverse reactions between oral immunotherapy protocols according to the dose increase method in patients with food allergy
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 3(Year) 至 17(Year)(—)
- 性别
- All
入选标准
- •? If one or more of eggs, milk, and wheat were positive in the food oral provocation test conducted within 12 months from the time of obtaining consent
- •? If food specific IgE (Uni-CAP) is 0.35 or higher within 12 months from the time of consent
- •? Subject and/or guardian consent to participate in the study
排除标准
- •* Patients who cannot stop taking drugs (systemic steroids, immunosuppressants, immunotherapeutics, biologics, etc.) that may affect the food oral provocation test and skin prick test for a period that may affect the test
- •* Patients who need to continue taking drugs that may aggravate symptoms during anaphylaxis (beta-blockers, angiotensin-converting enzyme (ACE) inhibitors, angiotensin-receptor blockers (ARB) or calcium channel blockers)
- •* Patients with severe cardiopulmonary disease requiring continuous treatment
- •* Patients with systemic diseases requiring a specific diet
- •* However, if anaphylaxis occurs after ingestion of eggs, milk, or wheat, it does not fall under the exclusion criteria.
研究者
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