NCT05083598已完成不适用
Wearable Health Technology for Perioperative Risk Assessment
Istituto Clinico Humanitas1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2021年6月10日最近更新:
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
- 试验地点
- 1
- 主要终点
- Assess whether wearable devices (WD) can identify patients at risk for postoperative complications.
研究概览
简要总结
Accurate and timely preoperative identification of high-risk patients provides opportunities to better inform and manage them. Current predictors for perioperative complications are either resource consuming or have low accuracy. The primary objective of the study is to assess if Wearable Devices may be an alternative to assess cardiopulmonary function, with low risks and lower costs.
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
- 70 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 70 or more
- •Undergoing major non cardiac surgery
- •Expected surgical duration > 2 hours.
排除标准
- •Patients unable to express consent
- •Patients undergoing urgent/emergent surgery
- •Patients in which surgery is planned within less than two weeks
- •Patients with limited physical activity due to limited mobility related with neurological or orthopedic disease
- •Acute cardiovascular event
- •Surgery conducted in locoregional anesthesia only
结局指标
主要结局
Assess whether wearable devices (WD) can identify patients at risk for postoperative complications.
时间窗: 12 months
次要结局
- A sub analysis of WD data during 6MWT will be conducted(24 months)
- To compare performance of WD data with 6MWT, MET scale, CFS and ASA score in identifying reduced functional capacity(24 months)
研究者
研究点 (1)
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