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Clinical Trials/ISRCTN58660550
ISRCTN58660550
Completed
未知

Does continuous monitoring of vital signs with an alerting system reduce length of hospital stay in post-operative upper gastro-intestinal surgery patients? A non-randomised study

Oxford University Hospitals NHS Foundation Trust0 sites407 target enrollmentAugust 11, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Oxford University Hospitals NHS Foundation Trust
Enrollment
407
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

2018 results in https://pubmed.ncbi.nlm.nih.gov/30096079/ (added 26/11/2020)

Registry
who.int
Start Date
August 11, 2017
End Date
December 31, 2014
Last Updated
5 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Oxford University Hospitals NHS Foundation Trust

Eligibility Criteria

Inclusion Criteria

  • 1\. All patients admitted to the Oxford Radcliffe Hospitals NHS Trust for Upper Gastro\-Intestinal Surgery. This will include patients undergoing the following procedures: oesophagectomy, oesophagogastrectomy, gastrectomy, whipples, liver resection, pancreatectomy, gastric bypass, billiary reconstruction and splenectomy.
  • 2\. Willing and able to give consent

Exclusion Criteria

  • 1\. Patients refusing consent
  • 2\. Children (less than 16 years old)
  • 3\. Prisoners
  • 4\. Pregnant women
  • 5\. Patients whose anatomy precludes the use of the required monitoring
  • 6\. Patients who are judged to lack capacity at the time of consent
  • 7\. Patients who cannot understand written English and for whom no translator can be found

Outcomes

Primary Outcomes

Not specified

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