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临床试验/DRKS00029287
DRKS00029287已完成不适用

German PBC Cohort

niversitätsklinikum Leipzig0 个研究点目标入组 1,200 人开始时间: 2022年7月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,200

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 one(—)
性别
All

入选标准

  • PBC diagnosis, as demonstrated by the presence of at least two of the following three diagnostic factors: ALP, AMA, liver biopsy. Medication based treatment with at least one drug approved in Germany for the treatment of PBC. Availability of all following essential parameters at the initial diagnosis of PBC prior to the initiation of treatment with UDCA, 12 months after initiation of UDCA and if applicable at time point of secondary incomplete response: Platelet count, ALP, Total Bilirubin, AST/GOT, Age at initial diagnosis of PBC. Patients must meet criteria of one of the cohorts within this NIS. Written statement of consent.

排除标准

  • Current participation in a phase I to IV interventional clinical trial for PBC or current participation in another PBC registry

研究者

发起方
niversitätsklinikum Leipzig

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