跳至主要内容
临床试验/DRKS00024724
DRKS00024724招募中不适用

TriMaximize: A multicentre, prospective, non-interventional trial monitoring therapy pathways of Asthma patients treated with an extra-fine ICS/LABA/LAMA single-inhaler triple therapy in a real-world setting and characterizing the effects on health-related outcomes - TriMaximize

Chiesi GmbH0 个研究点目标入组 3,950 人开始时间: 2021年3月25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
Chiesi GmbH
入组人数
3,950

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

  • 1) Patients = 18 years of age,
  • 2) Patients with confirmed leading diagnosis of asthma with or without concomitant COPD,
  • 3) Physician decision to start fixed triple therapy with ICS/LABA/LAMA (Trimbow® MS or HS) according to its current authorised indication. The treatment decision must be made independently from participation in
  • 4) Patients willing and able to sign an informed consent for use of their pseudonymised clinical data within the present non-interventional

排除标准

  • 1) Participation in an interventional clinical trial within 30 days prior to enrolment into the present non-interventional study or planned enrolment in an interventional clinical trial during the observational period.
  • No further selection criteria apply, in order to enrol a population that is likely to
  • reflect the current target population for ICS/LABA/LAMA combination therapy as per routine clinical practice.

研究者

发起方
Chiesi GmbH

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