跳至主要内容
临床试验/NCT02805114
NCT02805114已完成不适用

Obstructive Airways Diseases in Pulmonary Clinic (OADPC) Study

Oridion1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2016年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
Correlation between capnography parameters and severity of asthma

研究概览

简要总结

This is an observational study which aims to evaluate the possibility of using data from a capnography device to assess obstructive airway severity in both Chronic Obstructive Pulmonary Disease (COPD) and Asthma patients.

详细描述

This is an observational study which aims to evaluate the possibility of using data from a capnography device to assess obstructive airway severity in both COPD and Asthma patients. The study will include adult asthma and COPD patients (age >18). Patients will be enrolled on a continuous basis and will be monitored by capnograph and oximeter before and after lung function assessment and also during and after medical treatment.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ability and willingness to participate the study and sign informed consent form
  • Asthma / COPD patients

排除标准

  • Pregnant women
  • Asthma or COPD patients with FEV1 > 80%
  • Disability or unwillingness to undergo capnography measurement
  • Cannot be assessed for FEV1
  • Oxygen supply >5 L/min
  • Subjects that gone through LOBECTOMY OF LUNG in the last 5 years.

结局指标

主要结局

Correlation between capnography parameters and severity of asthma

时间窗: 1/2 hour to 48 hours from enrollment of subjects

Correlation between the airway obstruction severity calculation based on the capnography parameters and the clinical severity of asthma and COPD as defined by forced expiratory volume in 1 second (FEV1), in severe asthma and COPD patients

次要结局

未报告次要终点

研究者

发起方
Oridion
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验