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Clinical Trials/NCT03438578
NCT03438578
Completed
Not Applicable

Use of Efficacy Safety Score in Postoperative Management: A Prospective, Randomized Study

St. Olavs Hospital1 site in 1 country200 target enrollmentMarch 5, 2018
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ConditionsPain, PostoperativePostoperative Nausea and Vomiting

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
St. Olavs Hospital
Enrollment
200
Locations
1
Primary Endpoint
Time to Mobilization
Status
Completed
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
March 5, 2018
End Date
March 1, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
St. Olavs Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •undergoing surgery
  • •expectedly to be treated and observed in hospital for more than 24 hours postoperatively

Exclusion Criteria

  • •refusal of participation
  • •poor communication capabilities

Outcomes

Primary Outcomes

Time to Mobilization

Time Frame: 24 hours

The measured postoperative time when patient can stand and able to walk one or more steps, with or without support

Secondary Outcomes

  • Pain Measurement, Verbal Numeric Rating Scale(24 hours)
  • Patient Satisfaction(24 hours)

Study Sites (1)

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