Inhospital Resuscitation: Incidence, Causes and Outcome

March 14, 2024 updated by: Sule Ozbilgin, Dokuz Eylul University

Causes and Outcome of Cardiac Arrest In-a University Hospital

Define the frequency and survival pattern of cardiac arrests in relation to the hospital day of event and etiology of arrest.

Study Overview

Status

Withdrawn

Detailed Description

Define the frequency and survival pattern of cardiac arrests in relation to the hospital day of event and etiology of arrest.

The study aims to evaluate the outcome of in-hospital cardiac arrests, focusing on the relationship between etiology and outcome and, in particular, in relation to the length of hospitalization prior to the cardiac arrest. The aimed to sought to test the hypothesis that cardiac arrests occurring after longer hospitalizations were associated with lower survival rates and worse neurological outcomes compared to shorter hospitalizations.

Study Type

Observational

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

      • İzmir, Turkey, 35340
        • Dokuz Eylül University, School of Medicine, Department of Anesthesiology and Intensive Care

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

Sampling Method

Probability Sample

Study Population

This study will include all patients who develop cardiac arrest in the hospital(Dokuz Eylul University Hospital).

Description

Inclusion Criteria:

  • Cases where the emergency help team is called

Exclusion Criteria:

  • Absence of informed consent
  • Lack of data records of patients

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
incidence of in hospital cardiac arrest
Time Frame: baseline
baseline
neurologic outcome of patients according to Cerebral performance category scale
Time Frame: until six months after return of spontaneous circulation
The Cerebral performance category scale ranges from 1 to 5 with 1 representing intact function and 5 representing brain death.
until six months after return of spontaneous circulation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
causes of intraoperative cardiac arrest among participants/patients
Time Frame: baseline
Probable causes of intraoperative cardiac arrest among participants/patients Diabetes, Hypertension, Smoking, Dyslipidemia, Coronary artery disease, Chronic respiratory insufficiency, Chronic heart failure, Chronic renal insufficiency, Chronic hepatic insufficiency, Chronic neurological disease, Cancer.
baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Sule Ozbilgin, Dokuz Eylül University, School of Medicine, Department of Anesthesiology and Intensive Care

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)

July 1, 2014

Primary Completion (Estimated)

April 1, 2024

Study Completion (Estimated)

May 1, 2024

Study Registration Dates

First Submitted

December 20, 2017

First Submitted That Met QC Criteria

December 20, 2017

First Posted (Actual)

December 27, 2017

Study Record Updates

Last Update Posted (Actual)

March 15, 2024

Last Update Submitted That Met QC Criteria

March 14, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 153-GOA

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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