临床试验/ISRCTN61535692

ISRCTN61535692已完成未知

Virtual HDU: hypoxia study. Accuracy and validity testing of ambulatory monitoring system

niversity of Oxford0 个研究点目标入组 29 人开始时间: 2019年6月10日最近更新: 2023年8月2日

试验速览

阶段: 未知
状态: 已完成
发起方: niversity of Oxford
入组人数: 29

研究概览入排标准研究者记录与标识符相似试验

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

发起方

niversity of Oxford

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