Cardiopulmonary Resuscitation in Operating Room

Intraoperative Cardiac Arrest Clinical Trial

— CPR  

Official title:

Intraoperative Cardiac Arrest: Incidence and Outcome

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02884271
• Other study ID #: 2482-GOA
• Status: Recruiting
• Start date: March 2016
• Est. completion date: May 2027

Study information

• Verified date: February 2024
• Source: Dokuz Eylul University
• Contact: Bahar Kuvaki, Professor
• Phone: 902324122836
• Email: bkuvaki[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 7
• Est. completion date: May 2027
• Est. primary completion date: December 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

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

Related Conditions & MeSH terms

• Heart Arrest
• Intraoperative Cardiac Arrest

Intervention

Procedure:
• cardiopulmonary resuscitation
start cardiopulmonary resuscitation

Locations

Country	Name	City	State
Turkey	Dokuz Eylül University, School of Medicine, Department of Anesthesiology and Reanimation	Izmir

Sponsors (1)

Lead Sponsor	Collaborator
Dokuz Eylul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	incidence of intraoperative cardiac arrest		baseline
Primary	neurologic outcome of patients according to Cerebral performance category scale		until six months after return of spontaneous circulation
Secondary	causes of intraoperative cardiac arrest among participants/patients	Probable causes of intraoperative cardiac arrest among participants/patients; Trauma; End stage liver disease and complications associated with liver transplantation; Unable to wean from cardiopulmonary bypass; Complications associated with cardiac surgery; Ruptured aneurysm; abdominal or thoracic; Technical complications: surgical and special procedures, central venous access; Complications associated with automatic implantable cardiac defibrillator placement; Hemorrhage; Complications associated with radical cancer surgery; Sepsis and multiple organ failure; Perioperative myocardial infarction; Complications associated with congenital heart defect; Complications associated with neurosurgery; Complications associated with Anaesthesia (anaphylaxis, difficult airway management/difficult ventilation, adverse drug, total spinal anaesthesia/bloc etc)	baseline