Crome/Cobalt Respiration Study
不适用
已完成
NCT06089694
| 适应症 | Heart Failure |
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| 分期 | 不适用 |
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| 申办方 | Medtronic Cardiac Rhythm and Heart Failure |
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| 状态 | 已完成 |
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| 受试者人数 | 61 人 |
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| 干预(药物) | Enabling Sensor Research Holter Mode feature |
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| 开始日期 | 2023年11月21日 |
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| 完成日期 | 2024年6月12日 |
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| 结果公布日 | 2026年7月21日 |
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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 Subjects | 15.3 ± 3.7 breaths per minute |
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Daily Device-derived Respiration Rate
During In-clinic Testing Visit, an average of 2 hours · breaths per minute
| All Enrolled Subjects | 15.5 ± 3.5 breaths per minute |
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Difference in Respiration Rate
During In-clinic Testing Visit, an average of 2 hours · breaths per minute
| All Enrolled Subjects | 0.2 ± 1.1 breaths per minute |
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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。