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Heart Arrest clinical trials

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NCT ID: NCT02367755 Recruiting - Cardiac Arrest Clinical Trials

Therapeutic Hypothermia With Propofol in Survival and Neurological Prognoses After Cardiac Arrest

Start date: August 2013
Phase: Phase 4
Study type: Interventional

Therapeutic hypothermia has been proven to significantly improve the survival and neurological prognoses in patients resuscitated from cardiac arrest. Propofol has been reported to exhibit potentials in mitigating ischemia-reperfusion injury via the antioxidative, anti-inflammatory and neuroprotective mechanisms. This study is to investigate the potentials of propofol in further improving the survival and neurological prognoses in this era of therapeutic hypothermia.

NCT ID: NCT02344693 Recruiting - Cardiac Arrest Clinical Trials

Electroencephalography in Patients Resuscitated From Cardiac Arrest

Start date: August 1, 2017
Phase:
Study type: Observational [Patient Registry]

Sudden cardiac death can occur due to a multitude of causes. The underlying case can affect the overall prognosis. A return of spontaneous circulation not exceeding 30 minutes following a successful cardiopulmonary resuscitation is usually deemed imperative, if the patient is to survive. Monitors for evaluating the cardiac function during and after resuscitation are implemented on a daily basis (ekg, pulseoxymetry, blood pressure monitoring, cardiac sonography), but no devices for registration of the cortical brain activity exist. The aim of this study is to provide a 3-channel electroencephalogram using a prototype EEG/EKG adapter, connected to a Physio-Control LifePak 15 monitor/defibrillator, in patients who regain spontaneous circulation following non-traumatic cardiac arrest.

NCT ID: NCT02326506 Recruiting - Heart Arrest Clinical Trials

Evaluation of Drainable Volume Measurements During VA-ELS

Start date: September 2014
Phase: N/A
Study type: Interventional

Veno-arterial extracorporeal life support (VA-ELS) is used to support patients with acute cardiac failure. In that context, sufficient drainable venous volume is crucial for reliable and adequate support. To date, no reliable measurement method exists to monitor drainable volume adequately. Furthermore, it is still unresolved how to diagnose adequate cardiac recovery. Previous (pre)clinical studies showed that the calculation of the dynamic filling index may provide a valuable parameter to monitor the drainable volume in patients supported by VAELS. In addition, a case report showed that measurement of the dynamic filling index could successfully be used to estimate cardiac recovery in a single patient supported by VA-ELS in the ICU. This study will assess the dynamic filling index as a representation for drainable volume and cardiac recovery using standard recorded perfusion data in patients supported by VA-ELS

NCT ID: NCT02309151 Recruiting - Clinical trials for Out-of-Hospital Cardiac Arrest

Direct or Subacute Coronary Angiography in Out-of-hospital Cardiac Arrest

DISCO
Start date: December 2014
Phase: N/A
Study type: Interventional

The overall aim of this prospective, randomized study is to investigate whether acute coronary angiography (within 120 minutes) with a predefined strategy for revascularization, will improve 30-day survival in patients with out of hospital cardiac arrest with no signs of ST-elevation on ECG after Restoration of Spontaneous Circulation (ROSC). The patients will be randomized to a strategy of immediate coronary angiography within 120 minutes or to a strategy of delayed angiography that may be performed three days after the cardiac arrest.

NCT ID: NCT02305524 Recruiting - Cardiac Arrest Clinical Trials

Intubation During Adult Intubation

SLETI
Start date: November 2014
Phase: N/A
Study type: Interventional

The objective of this study is to compared effectiveness of intubation using ETView VivaSight SL and standard tracheal tube during resuscitation performed by a EMS-paramedics.

NCT ID: NCT02305511 Recruiting - Cardiac Arrest Clinical Trials

Intraosseous Access During Pediatric Resuscitation

IOCPR
Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study was to compare the Jamshidi, the BIG, the Cook, the EZIO intraosseous devices to standard peripheral venous catheterization during pediatric resuscitation.

NCT ID: NCT02297776 Recruiting - Cardiac Arrest Clinical Trials

Circulating Biomarkers Predict Neurological Outcome After Cardiac Arrest

CABNO
Start date: August 2014
Phase: N/A
Study type: Observational

Prediction of clinical outcome after cardiac arrest is clinically important.Early prognostication after successful cardiopulmonary resuscitation is difficult, and there is a need for novel methods to estimate the extent of brain injury and predict outcome. In this study, the investigators will evaluate the plasma levels of microRNAs (miRNAs) and circRNAs after cardiac arrest and assessed their ability to prognosticate neurological outcome.

NCT ID: NCT02295670 Recruiting - Cardiac Arrest Clinical Trials

Pediatric Difficult Intubation

3V-L DL
Start date: November 2014
Phase: N/A
Study type: Interventional

Endotracheal intubation (ETI) is perceived as the optimal method of providing and maintaining a clear and secure airway. The 2010 European Resuscitation Council (ERC) guidelines emphasized the importance of minimal interruption during cardiopulmonary resuscitation (CPR). These guidelines also suggest that skilled operators should be able to secure the airway without interrupting chest compression. The aim of the study was to compare time and success rates of the Vividtrac video-laryngoscope and the Miller laryngoscope for emergency intubation during simulated pediatric CPR.

NCT ID: NCT02295657 Recruiting - Cardiac Arrest Clinical Trials

Double Lumen Tube Intubation

DLETI
Start date: November 2014
Phase: N/A
Study type: Interventional

The aim of this study was to compare time, success rates of different double-lumen tubes in intubation in a standardized manikin model.

NCT ID: NCT02295631 Recruiting - Cardiac Arrest Clinical Trials

ETI During Spinal Trauma

Start date: November 2014
Phase: N/A
Study type: Interventional

The aim of this study was to compare time, success rates of different tracheal tubes (standard tube and ETView VivaSight SL) for intubation with an immobilized cervical spine in a standardized manikin model.