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Recruiting NCT02884271

Cardiopulmonary Resuscitation in Operating Room

— Observational Intraoperative Cardiac Arrest

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: cardiopulmonary resuscitation.
Who it may be relevant to
Registry conditions: Intraoperative Cardiac Arrest. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Intraoperative Cardiac Arrest: Incidence and Outcome

Overview

In the last ten years patient safety during routine surgical interventions has increased; however as there is an increase in the number of specialized surgical interventions and high risk patients like elderly and emergency patients, the incidence of perioperative cardiac arrest has not reduced but remains fixed. The incidence of perioperative cardiac arrest varies from 4.3-34.6 for each 10,000 procedures. However as in a lot of other countries exact data are lacking also for Turkey. With this study the investigators want to start collecting data about intraoperative cardiac arrest in Turkey, starting at their institution The aim is to evaluate the incidence and outcome in the study. Secondary aim is to assess the causes of cardiac arrest in the operating room.

Detailed description

Patient information will be collected on a form entitled "Data collection form" including all medications and interventions during cardiopulmonary resuscitation and routine daily used anesthesia registration form.

Interventions

  • Procedure cardiopulmonary resuscitation
    start cardiopulmonary resuscitation

Primary outcome measures

  • incidence of intraoperative cardiac arrest [Time frame: baseline]
  • neurologic outcome of patients according to Cerebral performance category scale [Time frame: until six months after return of spontaneous circulation]
Secondary outcome measures (1)
  • causes of intraoperative cardiac arrest among participants/patients [Time frame: baseline]

Eligibility criteria

Inclusion criteria

  • All patients who develop cardiac arrest in the operating room

Exclusion criteria

  • Absence of informed consent
  • Patients arriving into the operating room with ongoing CPR

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Turkey (Türkiye) · 1 center
  • Dokuz Eylül University, School of Medicine, Department of Anesthesiology and Reanimation — Izmir

Identifiers

NCT: NCT02884271 · 2482-GOA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗