NCT07051421

Brief Summary

In this study, we aimed to develop a scoring system that facilitates patient risk stratification in the recovery room during the postanesthetic follow-up period and can objectively identify patients in need of early intervention.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
208

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

July 1, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 4, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

July 4, 2025

Status Verified

June 1, 2025

Enrollment Period

4 months

First QC Date

June 26, 2025

Last Update Submit

June 26, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • RECO-EWS

    0-7 low risk, 7-10 medium risk, ≥10 high risk

    24 HOURS

Interventions

In the RECO-EWS scoring system we designed; 0-7 low risk, 7-10 medium risk, ≥10 high risk, postoperative stay findings of high-risk patients and, if necessary, new cut-off values are determined for each parameter in the scoring system according to the analysis results.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients over 18 years of age, in ASA class I-III, who have undergone planned elective surgery under general anesthesia, and who have been informed and given informed consent in advance of the study.

You may qualify if:

  • Those over 18 years of age,
  • Those in ASA I-III class,
  • Those who have undergone planned elective surgery under general anesthesia,
  • Those who have been informed about the study in advance and given their consent.

You may not qualify if:

  • Those under 18 years of age,
  • Those who underwent emergency intervention,
  • Those in the ASA-Ⅳ class,
  • Those who underwent regional anesthesia,
  • Those with a history of cognitive retardation, visual-hearing impairment or psychiatric disease that prevents communication, those who have previously been diagnosed with neurocognitive disorders,
  • Patients who could not complete the procedure, patients with data loss,
  • Patients whose general anesthesia duration is less than 90 minutes will not be included in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Pazar B, Yava A. Evaluation of Early Warning Scoring System and Nursing Guide Application in Post-Anaesthesia Care Unit. Turk J Anaesthesiol Reanim. 2013 Dec;41(6):216-22. doi: 10.5152/TJAR.2013.37. Epub 2013 May 23.

  • Mert S, Kersu O, Cesur S, Topbas O, Erdogan S. The Effect of Modified Early Warning Score (MEWS) and Nursing Guide Application on Postoperative Patient Outcomes: A Randomized Controlled Study. J Perianesth Nurs. 2024 Aug;39(4):596-603. doi: 10.1016/j.jopan.2023.10.023. Epub 2024 Feb 1.

MeSH Terms

Interventions

Early Warning Score

Intervention Hierarchy (Ancestors)

Severity of Illness IndexPatient AcuityHealth Status IndicatorsHealth SurveysSurveys and QuestionnairesData CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
ASSOC.PROF.

Study Record Dates

First Submitted

June 26, 2025

First Posted

July 4, 2025

Study Start

July 1, 2025

Primary Completion

November 1, 2025

Study Completion

December 1, 2025

Last Updated

July 4, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share