N/A
Completed N=200
Efficacy Safety Score in Postoperative Management
Pain, Postoperative · Postoperative Nausea and Vomiting
Source: ClinicalTrials.gov NCT03438578 ↗
Enrolled (actual)
200
Serious AEs
1.0%
Results posted
Sep 2020
Primary outcomePrimary: Time to Mobilization — 10.1; 14.2 hours
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.
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 | — |
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. Informational only — not medical advice.