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临床试验/ISRCTN56492264
ISRCTN56492264已完成未知

An exploratory, observational clinical evaluation of the CRiL N­-Tidal C data-collector capnometer to collect breathing records in patients with COPD

Cambridge Respiratory Innovations Ltd0 个研究点目标入组 30 人开始时间: 2016年6月13日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
30

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

性别
All

入选标准

  • 1. Patients of either sex, age 18 years and over, diagnosed with COPD, who have given written, informed consent
  • 2. Patients in the case-managed group will have chronically elevated partial pressure of
  • carbon dioxide (PaCO2) and will be susceptible to frequent exacerbations of COPD
  • 3. Patients in the acute admission group will have been admitted to hospital via the emergency room for treatment of COPD­related ventilatory failure

排除标准

  • 1. Diagnosis of neuromuscular disorders or kyphoscoliosis
  • 2. Patients who, in the opinion of the investigator are unlikely to comply with the requirements of the study,
  • use the device correctly, or keep the diary records

研究者

发起方
Cambridge Respiratory Innovations Ltd

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