Clinical pilot study to find agreement between the respiratory rates obtained by raybaby with HCGs respiration monitor equipment (GE B30 patient monitor)
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- To check the agreement between the respiratory rates between the GE B30 and raybaby among adults, aging between 18 to 80 in the intensive care unit.
研究概览
简要总结
This is an observational study to evaluate the effectiveness of Raybaby breathing monitor with respect to a medically certified device to assess the suitability of Raybaby non contact breath monitoring technique for clinical use. The study is yet to begin and publication would be drafted at the end of the study to establish correlation with medical standards and relevance.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 80.00 Year(s)（—）
- 性别
- All
入选标准
- •General ICU patients.
排除标准
- •Patient with known lung issues.
结局指标
主要结局
To check the agreement between the respiratory rates between the GE B30 and raybaby among adults, aging between 18 to 80 in the intensive care unit.
时间窗: Respiratory rates (parameter of evaluation) from both devices will be compared at time intervals from 5 seconds or more and will be assessed post completion of monitoring of respective patients, starting from a minimum of 4 hour. Observations will be compiled every 2 weeks.
次要结局
- To obtain usable respiration data with an average of 20% conversion rate from 4 to 10 hours of monitoring patients at periodic intervals of 5 minutes.