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L'essai clinique NCT02884271 (CPR) pour Intraoperative Cardiac Arrest est en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici.
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Cardiopulmonary Resuscitation in Operating Room (CPR)

En recrutement
Les détails de l'essai clinique sont principalement disponibles en anglais. Cependant, l'IA Trial Radar peut vous aider ! Cliquez simplement sur 'Expliquer l'essai' pour voir et discuter des informations sur l'essai dans la langue sélectionnée.
L'étude clinique NCT02884271 (CPR) est un essai observationnel pour Intraoperative Cardiac Arrest. Son statut actuel est : en recrutement. L'étude a débuté le 1 mars 2016 et vise à recruter 7 participants. Dirigé par Dokuz Eylul University, l'essai devrait être terminé d'ici le 1 mai 2027. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 20 février 2024.
Résumé succinct
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 détaillée
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.
Titre officiel

Intraoperative Cardiac Arrest: Incidence and Outcome

Conditions
Intraoperative Cardiac Arrest
Autres identifiants de l'essai
  • CPR
  • 2482-GOA
Numéro NCT
NCT02884271
Date de début (réel)
2016-03
Dernière mise à jour publiée
2024-02-20
Date de fin (estimée)
2027-05
Inscription (estimée)
7
Type d'essai
Observationnel
Statut
En recrutement
Mots clés
CPR
cardiac arrest
operating room
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
cardiac arrest group
patients who develop intraoperative cardiac arrest
Cardiopulmonary Resuscitation
start cardiopulmonary resuscitation
without cardiac arrest group
patients who don't develop intraoperative cardiac arrest
N/A
Critère principal d'évaluation
Critères d'évaluationDescription de critèresPériode
incidence of intraoperative cardiac arrest
baseline
neurologic outcome of patients according to Cerebral performance category scale
until six months after return of spontaneous circulation
Critère secondaire d'évaluation
Critères d'évaluationDescription de critèresPériode
causes of intraoperative cardiac arrest among participants/patients
Probable causes of intraoperative cardiac arrest among participants/patients 1. Trauma 2. End stage liver disease and complications associated with liver transplantation 3. Unable to wean from cardiopulmonary bypass 4. Complications associated with cardiac surgery 5. Ruptured aneurysm; abdominal or thoracic 6. Technical complications: surgical and special procedures, central venous access 7. Complications associated with automatic implantable cardiac defibrillator placement 8. Hemorrhage 9. Complications associated with radical cancer surgery 10. Sepsis and multiple organ failure 11. Perioperative myocardial infarction 12. Complications associated with congenital heart defect 13. Complications associated with neurosurgery 14. Complications associated with Anaesthesia (anaphylaxis, difficult airway management/difficult ventilation, adverse drug, total spinal anaesthesia/bloc etc)
baseline
Critères d'éligibilité

Âges éligibles
Enfant, Adulte, Adulte âgé
Sexes éligibles
Tous
  • All patients who develop cardiac arrest in the operating room

  • Absence of informed consent
  • Patients arriving into the operating room with ongoing CPR
Dokuz Eylul University logoDokuz Eylul University
Partie responsable de l'essai
Sule Ozbilgin, Investigateur principal, Staff anesthesiologists in Department of Anaesthesiology and Intensive Care in Dokuz Eylul Universty Hospital, Dokuz Eylul University
Contact central de l'essai
Contact: Bahar Kuvaki, Professor, 902324122836, [email protected]
Contact: Sule Ozbilgin, MD, 905055252901, [email protected]
1 Centres de l'essai dans 1 pays
Dokuz Eylül University, School of Medicine, Department of Anesthesiology and Reanimation, Izmir, 35340, Turkey (Türkiye)
Bahar Kuvaki, Professor, Contact, 902324122836, [email protected]
Sule Ozbilgin, MD, Contact, 905055252901, [email protected]
En recrutement