JPRN-jRCT1050220128进行中（未招募）Unknown
Patient prognosis evaluation with retrospective data in severe perinatal, benign perinatal or infantile HPP: A pooled analysis from the post-marketing study and perinatal findings surveillance - HPP-PERINATAL study
Sawai Hideaki0 个研究点目标入组 40 人开始时间: 2022年12月8日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 40
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
- ot applicable 至 ot applicable（—）
- 性别
- All
入选标准
- •1. At the time of the PMS data lock in July 2021, Strensiq Specified drug use-results survey (post-marketing survey) Patients should have have provided data to PMS prior the data base lock date above.
- •2. Patients diagnosed with perinatal severe hypophosphatasia, perinatal benign hypophosphatasia, or infantile hypophosphatasia
- •3. A patient whose legal representative or patient can give written consent to provide patient information and a patient whose mother can give written consent to provide maternal information.
排除标准
- •1. Patients diagnosed with non-perinatal and non-infantile hypophosphatasia
- •2. Patients in whom fetal ultrasound image data including the number of weeks of gestation before and after 28 ~ 31 weeks of gestation cannot be obtained
研究者
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