TCTR20210514006招募中不适用
Incidence of genetic abnormalities in patients with primary hypereosinophilia
Siriraj Hospital Mahidol University0 个研究点目标入组 151 人开始时间: 2021年5月14日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 151
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
- 18 Years 至 N/A (No limit)(—)
- 性别
- All
入选标准
- •1) The patients diagnosed with primary hypereosinophilia type white blood cells greater than 1,500 per microliter for a period of more than 1 month
- •2) 18 years of age and over
- •3) Patients who received the gene test The specific targeted fusion gene panel with hypereosinophilia
- •4) was welcomed to join the program by signing.
排除标准
- •1.The patient was detected from a bacterial infection by antibody detection Research projects in which patients are examined. Incidence of nasopharyngeal carcinoma in patients primary hypereosinophilias 686 / 2563 (IRB2)
- •2.Patients with allergic history
- •3.Asthma patients
- •4. Patients with immune diseases
- •5 Patients diagnosed with various cancers are not in peacetime.
- •6. History of steroid use in patients with herbs or drugs in the past three months
- •7. The patients had a history of adverse events leading to leukocyte disease, hypertension, and xa0;
- •Penicillin, cephalosporin, GM-CSF, NSAID, ranitidine, isopropanol, isopropanol, alanine, amazillin sulfate, chlorazine, chlorazine Cyclospora
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