ISRCTN17105027已完成未知
Predicting vasovagal and other adverse events in Australian voluntary blood donors using a portable sensor that measures bio-signal data (PREVENT)
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 522
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
- 性别
- All
入选标准
- •1. Eligible to donate as per the Australian Red Cross Lifeblood Guidelines for the Selection of Blood Donors
- •2. Donating whole blood or plasma for the first time
- •3. Willing and able to provide informed consent
- •4. Has a plasma or whole blood appointment at one of the participating donor centres (appointment made as a walk-in donor or scheduled appointment)
排除标准
- •1. Unwilling or unable to provide informed consent
- •2. Lack of understanding of the English language necessary to complete questionnaires. This study will not use translation services or interpreters
- •3. Contacted for a research study in the last 6 months as per Lifeblood contact policy
- •4. Donors with therapeutic, autologous, sample or platelet donation appointments
- •5. Lifeblood employees
研究者
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