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Cardiac Arrest clinical trials

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NCT ID: NCT02381977 Completed - Stroke Clinical Trials

Prevalence of Acute Critical Neurological Disease in Children: a Global Epidemiological Assessment

PANGEA
Start date: November 2011
Phase: N/A
Study type: Observational

PANGEA is an international prospective point prevalence study to describe the epidemiology, interventions, and outcomes in children with acute critical brain disease.

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: 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: NCT02295618 Completed - Cardiac Arrest Clinical Trials

ETI During Intubation

SL
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 novice-physicians.

NCT ID: NCT02291653 Completed - Cardiac Arrest Clinical Trials

Pediatric Endotracheal Intubation

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

We hypothesized that the McGrath MAC EMS is beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of the McGrath MAC EMS and MIL laryngoscopes in child resuscitation with and without CC.

NCT ID: NCT02289872 Completed - Cardiac Arrest Clinical Trials

Pediatric Intubation

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

The aim of the study was to compare time and success rates of TruView PCD video laryngoscope and Macintosh laryngoscope for the pediatric emergency intubation with three airway scenarios in a standardized manikin model.

NCT ID: NCT02281903 Completed - Cardiac Arrest Clinical Trials

Pediatric Resuscitation With Feedback CPR Devices

PRFD
Start date: October 2014
Phase: N/A
Study type: Interventional

The aim of this study was to compare the TrueCPR feedback device (with metronome) to standard basic life support (BLS) in terms of the quality of single rescuer pediatric resuscitation. Therefore, our hypothesis was that there would be no difference between both CPR methods in terms of chest compression quality parameters.

NCT ID: NCT02275234 Completed - Cardiac Arrest Clinical Trials

Care After Resuscitation

CARE
Start date: September 2014
Phase:
Study type: Observational

The purpose of this study is to investigate whether simple psychological interventions can be implemented at the Essex Cardiothoracic Centre (CTC) with a view to supporting the psychological wellbeing of survivors of cardiac arrest during their recovery.

NCT ID: NCT02260258 Completed - Cardiac Arrest Clinical Trials

Neuromuscular Blockade for Post-Cardiac Arrest Care

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

The main purpose of this study is to evaluate if neuromuscular blockade improves lactate clearance (and preliminary secondary clinical outcome measures) as compared to usual care in post-cardiac arrest patients undergoing targeted temperature management.