NL-OMON56095已完成不适用
COPD monitoring - COPD monitoring
niversitair Medisch Centrum0 个研究点目标入组 31 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 31
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 至 99（—）
入选标准
- •1.Subject must have a clinical diagnosis of COPD
- •2. mMRC (Modified Medical Research Council) Dyspnea Scale Score > 1
- •3. Subject must be indicated for regular inpatient/outpatient pulmonary
- •rehabilitation at CIRO
- •4. Subject must be willing to provide Informed Consent for their participation
- •in the study
- •5. Subject must be >=18 years of age
排除标准
- •1. Subjects who are unable/unwilling to voluntarily participate in the study
- •2.Subjects who cannot read/write
- •3. Subject has congenital heart disease
- •4.Subject has unstable coronary artery disease
- •5.Subject has an active implanted cardiac device (i.e. IPG, ICD)
- •6.Subject has heart failure NYHA 4
- •7.Subject presents any concomitant condition which in the opinion of the
- •investigator would not allow a safe participation in the study
- •8.Subject is legally incompetent
- •9.Subject is pregnant or has suspect to be pregnant
- •10.Subject is enrolled in a concurrent study that may confound the results of
- •this study without documented pre-approval from Medtronic study manager
- •11. BORG scale assessment is evaluated as unreliable due to patient*s cognitive
研究者
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