跳至主要内容
临床试验/ISRCTN51530527
ISRCTN51530527暂停未知

Virtual HDU Phase 4: Ambulatory monitoring system user interface integration and development.

niversity of Oxford0 个研究点目标入组 78 人开始时间: 2019年7月26日最近更新:

试验速览

阶段
未知
状态
暂停
入组人数
78

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

  • Stage A: Staff Focus Group/Interviews
  • 1. Any clinical staff member who uses SEND or measures patient vital signs
  • Study B: Locational testing of AMS
  • 1. Willing and able to give informed consent for participation in the study.
  • 2. Aged 18 years or above.
  • 3. Admitted to a surgical emergency unit (including post-ICU patients) and not currently monitored with continuous monitoring
  • Study C: Usability Testing
  • 1. Any clinical staff member who uses SEND and measures patient vital signs
  • 2. Any staff member who may be an end user of a AMS-SEND system

排除标准

  • Stage A: Staff Focus Group/Interviews
  • 1. Any staff member who cannot give informed consent
  • Stage B: Locational testing of AMS
  • 1. Allergies to nickel.
  • 2. Intra-cardiac device
  • 3. Already on continuous monitoring
  • 4. Diagnosed dementia
  • Stage C: Usability testing
  • 1. Any staff member who cannot give informed consent

研究者

相似试验

进行中(未招募)
Unknown
Home monitoring for acutely unwell patients being managed at home as part of a virual ward care pathway: a feasibility studyAcutely unwell patients receiving care from the Oxford University Hospital (OUH) acute hospital-at-home servicesSigns and Symptoms
ISRCTN11298549niversity of Oxford35
进行中(未招募)
不适用
A Phase IV, Multi-Center, Active-Controlled, Observer-Blind Study to Evaluate the Safety of a Trivalent Subunit Influenza Vaccine Produced either in Mammalian Cell Culture (Optaflu®) or in Embryonated Hen Eggs (Agrippal®) in Adults and Elderly With and Without Underlying Medical Conditions, and to Evaluate the Immunogenicity in a Subset of Subjects With Underlying Medical Conditions.no medical condition: healthy subjects
EUCTR2007-002872-32-DEovartis Vaccines and Diagnostics S.r.l.
已完成
不适用
A Multicenteric study to estimate the burden of rotavirus gastroenteritis among hospitalization due to diarrhea.
CTRI/2012/03/002475Shantha Biotechnics Limited2,000
进行中(未招募)
1 期
A Phase IV, Single-Centre, Observer-Blind, Controlled, Randomized Study to Compare the Safety and Immunogenicity of Fluvirin® to Influvac® Administered to Healthy Children 3 to 12 Years of Age. - Fluvirin Paediatric Trial
EUCTR2006-002649-35-GBovartis Vaccines and Diagnostics S.r.l.
尚未招募
4 期
Hospital centralized monitoring of clinical safety of Shenkang Injection after marketing/A
ITMCTR2100005034The First Affiliated Hospital of He'nan University of Chinese Medicine