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Clinical Trial Summary

The primary aim of this project is to determine whether postoperative patients may benefit from the Efficacy Safety Score (ESS) as a tool for postoperative clinical decision support, with a special focus on the first 24 hours after discharge from the postoperative care unit.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03438578
Study type Interventional
Source St. Olavs Hospital
Contact
Status Completed
Phase N/A
Start date March 5, 2018
Completion date March 1, 2019

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