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Efficacy Safety Score in Postoperative Management

NCT03438578 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2020-09-24

Study results available
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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.

Conditions

  • Pain, Postoperative
  • Postoperative Nausea and Vomiting

Interventions

DEVICE

Efficacy Safety Score monitoring

According to data gathered from ESS and monitoring, the patients will receive needed care.

Sponsors & Collaborators

  • Norwegian University of Science and Technology

    collaborator OTHER

  • St. Olavs Hospital

    lead OTHER

Principal Investigators

  • Johan Raeder, Prof · University of Oslo

  • Erik Solligård, MD PhD · St. Olavs Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-05
Primary Completion
2018-10-18
Completion
2019-03-01

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03438578 on ClinicalTrials.gov