BENITIONSClinical Trial Intelligence

Crome/Cobalt Respiration Study

不适用 已完成 NCT06089694

适应症Heart Failure
分期不适用
申办方Medtronic Cardiac Rhythm and Heart Failure
状态已完成
受试者人数61 人
干预(药物)Enabling Sensor Research Holter Mode feature
开始日期2023年11月21日
完成日期2024年6月12日
结果公布日2026年7月21日

摘要

The goal of this study is to compare measured respiration rates in various subject scenarios and use conditions between capnography and the Crome and Cobalt ICD and CRT-D MRI SureScan devices (derived using a Holter recorder).

Daily Capnography Respiration Rate

During In-clinic Testing Visit, an average of 2 hours · breaths per minute

All Enrolled Subjects15.3 ± 3.7 breaths per minute

Daily Device-derived Respiration Rate

During In-clinic Testing Visit, an average of 2 hours · breaths per minute

All Enrolled Subjects15.5 ± 3.5 breaths per minute

Difference in Respiration Rate

During In-clinic Testing Visit, an average of 2 hours · breaths per minute

All Enrolled Subjects0.2 ± 1.1 breaths per minute

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。