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临床试验/ISRCTN50251697
ISRCTN50251697已完成不适用

Comparison of goal-directed fluid optimisation guided by LiDCOrapid and conventional oesophageal Doppler ? effect on intra-operative oxygen delivery index and post-operative outcomes: a randomised control non-inferiority study

Guy's & St. Thomas' NHS Foundation Trust (UK)0 个研究点目标入组 336 人开始时间: 2012年9月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
336

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Elective or semi-elective patients due to undergo colorectal surgery as part of Enhanced Recovery Protocol
  • 2. Successful simultaneous LiDCOrapid and oesophageal Doppler monitoring throughout surgery

排除标准

  • 1. Emergency surgery
  • 2. Lack of capacity to consent
  • 3. Pregnancy
  • 4. All excluded patients from patient groups to be reported in results
  • 5. Contraindications to oesophageal Doppler probe
  • 5.1. nasal injuries or polyps
  • 5.2. severe oesophageal/laryngeal/pharyngeal disease
  • 5.3. recent oesophageal/laryngeal/pharyngeal surgery
  • 5.4. thoracic aortic aneurysm
  • 5.5. severe bleeding diathesis
  • 5.6. long-term systemic steroid therapy
  • 5.7. portal hypertension
  • 6. Contraindications to arterial line or LiDCOrapid
  • 6.1. weight <40kg
  • 6.2. aortic valve regurgitation

研究者

发起方
Guy's & St. Thomas' NHS Foundation Trust (UK)

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