NCT01434771撤回不适用
Simultaneous Hemodynamic and Ventilatory Monitoring Using Radio Frequency Impedance Interrogation (RFII), Thoracic Impedance Cardiography and Invasive Hemodynamic Monitoring Methods in Post Operative Cardiac Patients
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
研究概览
简要总结
The purpose of this study will be to compare standard of care invasive methods to an FDA approved non-invasive device and a novel wireless non-invasive device, both manufactured by Non-Invasive Medical Technologies Inc., with the goal of correlating the data generated by the novel device to the measurements taken by the standard of care invasive monitors.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 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
- 否
入选标准
- •18 years and older
- •Weight - 36-136 Kilograms
- •Height - 1.52 meters - 1.92 meters (5'- 6'4")
- •Scheduled for open heart surgery during the study period
排除标准
- •ECG lead adhesive allergy or sensitivity
- •Pregnant Patients
- •Prisoners
- •Cognitively impaired
- •Patients requiring mechanical cardiac support, or requirement for hemodialysis
- •Patients not requiring pulmonary artery catheters for medical management.
- •Patients with significant valvular disease will be enrolled if there is no significant post-repair valvular dysfunction as determined by intraoperative transesophageal echocardiography
研究者
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