NL-OMON53891尚未招募不适用
Clinical validation study of a wireless and wearable sensor for continuous vital signs monitoring in a clinical setting with vital sign ranges limited to the parameters recorded in a post anesthesia care unit - Clinical performance of a new wearable vital signs monitoring device
Fastfocus BV0 个研究点目标入组 20 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Adult patients (>18 years) (all sexes)
- •Surgical admission to hospital
- •At risk for transient perioperative desaturation (intermediate and major
- •Minimum expected duration at the recovery: at least 12 hours
- •(excluding day case surgery)
排除标准
- •Inability to give informed consent.
- •Planned primary post-operative admission to the Intensive Care Unit
- •Surgical location on - or close - to the ear
- •Patients with any of the contraindications (see section 4.3.1 of protocol
- •pagina 13)
- •Pregnant or breastfeeding women
研究者
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