Clinical Trials Logo

Cardiac Arrest clinical trials

View clinical trials related to Cardiac Arrest.

Filter by:

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: NCT02327871 Completed - Cardiac Arrest Clinical Trials

Esophageal Temperature Management After Cardiac Arrest

THE-COOL
Start date: December 2014
Phase: N/A
Study type: Interventional

To control patient's body temperature remains of major importance especially after cardiac arrest (CA). Therapeutic hypothermia (TH) targeted to 32-34°C is now recommended for most unconscious CA patients. However, available modalities for inducing TH have a number of technical (side effects), logistical (difficulties of placement), and financial (cost) barriers. The Esophageal Cooling Device (ECD) is a multi-chambered silicone heat exchanger placed in the esophagus providing highly efficient heat transfer to a patient. The ECD is a device that potentially improves the effectiveness of TH in minimizing the risks of existing methods (such as invasive cooling). Initial mathematical and animal studies have shown strong support for the efficacy and safety of the ECD. Placement of a naso-gastric probe is a systematic standard of care for all unconscious patients suffering from CA. The present study will replace the usual naso-gastric probe by the ECD that can be used for gastric suctioning as usually done in such patients. The aim of this prospective, interventional study is to assess the feasibility and safety of the ECD in resuscitated CA-patients and treated with 32-34°C targeted TH. The primary outcome is the feasibility of inducing, maintaining, and rewarming patients from TH using the ECD (cooling rate, rewarming rate, and the percent of time within goal temperature during the goal-temperature maintenance period). Evaluation of adverse events (including cardiac arrhythmias, severe bradycardia, myocardial infarction/re-infarction, dysphagia, odynophagia, aspiration pneumonia, non-aspiration pneumonia, esophageal reflux and injury, and esophagitis) will be closely monitored during the whole period of the targeted temperature management (secondary endpoint).

NCT ID: NCT02322359 Completed - Cardiac Arrest Clinical Trials

Compression Is Life In Cardiac Arrest - Fatigue Study

CILICA-FS
Start date: August 2014
Phase: N/A
Study type: Observational

Context: Chest compressions represent an important physical effort leading to fatigue and cardiopulmonary resuscitation quality degradation. Despite a known harmful effect of chest compressions interruptions, current guidelines still recommend provider switch every 2 minutes. Feedback impact on chest compressions quality during an extended cardiopulmonary resuscitation remains to be assessed. Study design: simulated prospective monocentric randomized crossover trial. Participants and methods: Sixty professionals rescuers of the pre-hospital care unit of University Hospital of Caen (doctors, nurses and ambulance drivers) are enrolled to performed 10 minutes of continuous chest compression on manikin (ResusciAnne®, Laerdal), twice, with and without a feedback device (CPRmeter®). Correct compression score (the main criterion) is defined by reached target of rate, depth and leaning at the same time (recorded continuously). Hypothesis: Feedback device delay fatigue effect arises during cardiopulmonary resuscitation.

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: NCT02303548 Completed - Cardiac Arrest Clinical Trials

Bicarbonate in Patients With Out-of-hospital Cardiac Arrest

Start date: October 2014
Phase: Phase 2
Study type: Interventional

A pilot study to evaluate the effect of sodium bicarbonate administration on cardiopulmonary resuscitation results and outcomes in cardiac arrest patient with severe metabolic acidosis.

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.