ISRCTN61535692已完成未知
Virtual HDU: hypoxia study. Accuracy and validity testing of ambulatory monitoring system
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 29
研究概览
简要总结
2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34524087/ results (added 21/09/2021) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35166690/ (added 16/02/2022) 2020 Protocol article in http://dx.doi.org/10.1136/bmjopen-2019-034404 (added 19/07/2023)
研究设计
- 研究类型
- Observational
入排标准
- 性别
- All
入选标准
- •1. Willing and able to give informed consent for participation in the study
- •2. Men and women aged 18 or over and in generally good health
排除标准
- •1. Allergies to adhesive dressings (such as bio-occlusive dressings or micropore) or local anesthesic (e.g. Lidocaine)
- •2. Intra-cardiac device (e.g. Permanent pacemaker) or previous wrist arterial line
- •3. Epilepsy
- •4. Angina, congenital heart disease or history of severe cardiopulmonary disease
- •5. History of anaemia (reported in the pre-screening telephone call) or Hb below 100 g/l on first test
- •6. Resting hypoxaemia (SpO2 <94%) or significant cardiopulmonary disease rendering exposure to alveolar hypoxia unsafe, as determined by the research physician
- •7. Pregnancy or breastfeeding
- •8. Clotting disorders and use of antiplatelet or anticoagulant medication (such as Aspirin)
- •9. Claustrophobia precluding spell in the hypoxic exposure
研究者
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