N/A
N=200
Efficacy Safety Score in Postoperative Management
Pain, Postoperative · Postoperative Nausea and Vomiting
Bottom Line
View on ClinicalTrials.gov: NCT03438578 ↗Enrolled (actual)
200
Serious AEs
1.0%
Results posted
Sep 2020
Primary outcome: Primary: Time to Mobilization — 10.1; 14.2 hours
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Efficacy Safety Score monitoring (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- St. Olavs Hospital
- Primary completion
- Oct 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Mobilization |
10.1; 14.2 | — |
| SECONDARY Pain Measurement, Verbal Numeric Rating Scale |
2.1; 3.3 | — |
| SECONDARY Patient Satisfaction |
4.9; 4.3 | — |
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.
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
Data sourced from ClinicalTrials.gov (NCT03438578). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.