IRCT20150125020786N3招募中1 期
Follow-up of Severe Congenital Neutropenia Patients Receiving PegGCSF (PD lasta); Study of Early and Late Drug Complications
Pouyesh Darou biopharmaceutical Co.0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 10
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 years 至 no limit（—）
- 性别
- All
入选标准
- •Adult patients and children with severe congenital neutropenia over 12 years
- •Severe Congenital Neutropenia Patients
- •Myeloid maturation arrest in bone marrow
- •Already successfully treated with Filgrastim
- •Negative mutation in GCSF receptor
- •Normal spleen and liver in abdominal sonography
- •Consent to Participate in study and sign inform consent
- •Cooperative patient for close follow-up
排除标准
- •Secondary neutropenia due to chemotherapy or other diseases
- •Life-threatening complications such as anaphylaxis or splenic rupture due to Filgrastim
- •Uncooperative patient for close follow-up
- •Severe Spleenomegaly
- •patients with other chronic diseases such as heart or hepatic disease or ...
研究者
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