The Charlson Comorbidity Index: Predicting Severity in Emergency Departments (Charlson)

March 30, 2020 updated by: Abdullah Osman KOCAK, Ataturk University

Objective: The Charlson Comorbidity Index (CCI) is a comorbidity scale used widely throughout the world. It uses patients' preoperative and intraoperative morbidity factors to evaluate morbidity and mortality risk. Though the CCI has widespread use, it has not been evaluated in patients attending at ES, and its relationship with patient readmission has not been shown previously. In this study, we aimed to show whether there is a correlation between the CCI value and the number of repeated admissions to emergency services and that the CCI value can be used as a predicted factor for the serious patients.

Matherials and Methods: This was a prospective observational cross-sectional study. Age, gender, vital signs of the patients who agreed to participate in the study was recorded. Numbers of emergency service applications in the last 6 months and CCI score have been recorded.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study showed that CCI score can be used for identify serious patient in emergency service.

Study Type

Observational

Enrollment (Actual)

1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Erzurum, Turkey, 25100
        • Abdullah Osman Kocak

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

all patients admitted to the emergency room

Description

Inclusion Criteria:

  • Admitted patients were told about the study, and those who agreed to participate were included

Exclusion Criteria:

  • Patients who did not wish to participate in the study
  • Patients who were unable to work or who had problems with consciousness
  • Patients with non-hospital cardiopulmonary arrest
  • Patients who had previously participated in the study (readmitted patients)
  • Patients who had accessed ES for the same or a similar complaint within the last seven days
  • < 18 years' old

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patient(hospitalized)
patients who are admitted to the emergency department and hospitalized.
observation
control(not hospitalized)
patients who are admitted to the emergency department and not hospitalized.
observation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
determine the severity of patients. to identify patients who need hospitalization. determine the severity of patients.
Time Frame: 2018
to identify patients who need hospitalization.
2018

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

October 1, 2018

Primary Completion (ACTUAL)

October 7, 2018

Study Completion (ACTUAL)

January 1, 2019

Study Registration Dates

First Submitted

March 26, 2020

First Submitted That Met QC Criteria

March 30, 2020

First Posted (ACTUAL)

March 31, 2020

Study Record Updates

Last Update Posted (ACTUAL)

March 31, 2020

Last Update Submitted That Met QC Criteria

March 30, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Ataturkuniversity

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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