At a glance
ClinicalIndex Comparison RecordN/ACompleted· 200 enrolled
Drug / intervention
Efficacy Safety Score monitoringdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Use of Efficacy Safety Score in Postoperative Management: A Prospective, Randomized Study
In Brief
A clinical study evaluating Efficacy Safety Score monitoring for Pain, Postoperative and Postoperative Nausea and Vomiting. Completed, enrolled 200 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesNorway
CollaboratorsNorwegian University of Science and Technology
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
First PostedFeb 2018
Enrollment StartMar 2018
Primary CompletionOct 2018
Study CompletionMar 2019
TodayJul 2026
First PostedFeb 19, 2018
Enrollment StartMar 5, 2018
Primary CompletionOct 18, 2018
Study CompletionMar 1, 2019
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 8.4 years ago
Interventions
Efficacy Safety Score monitoringdevice
According to data gathered from ESS and monitoring, the patients will receive needed care.