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临床试验/DRKS00023862
DRKS00023862已完成不适用

Impact of CFTR-modulation with elexacaftor/tezacaftor/ivacaftor on the exercise capacity, intestinal and respiratory microbiome, microbial and inflammatory metabolites in cystic fibrosis - IMMProveCFInflammation, Microbiome, Metabolome and physical Performance in Cystic Fibrosis

Zentrum für Kinder- und Jugendmedizin der Universitätsmedizin Mainz0 个研究点目标入组 84 人开始时间: 2021年6月25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
84

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
6 Years 至 100 Years(—)
性别
All

入选标准

  • Age 6 and older
  • - Confirmed diagnosis and mutation
  • - Planned to start medication with elexacaftor/tezacaftor/ivacaftor
  • - Written informed consent (from parent or legal guardian if underaged)
  • Or sex- and aged matched healthy control

排除标准

  • - Comorbidity which exclude therapy with elexacaftor/tezacaftor/ivacaftor (e.g liver or renal insufficiency)
  • - Respiratory infection at the start of treatment
  • - Acute therapy changes 21 days before starting therapy with elexacaftor/tezacaftor/ivacaftor
  • - Antibiotic treatment up to 3 weeks prior to study start

研究者

发起方
Zentrum für Kinder- und Jugendmedizin der Universitätsmedizin Mainz

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