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Heart Arrest clinical trials

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NCT ID: NCT03006484 Completed - Clinical trials for Inhospital Cardiac Arrest

Neurological Outcomes After In-Hospital Cardiac Arrest

NO-IHCA
Start date: March 21, 2017
Phase:
Study type: Observational

Little is known about the long-term neurological outcomes after in-hospital cardiac arrest (IHCA). It is also not known whether withdrawal of life-sustaining measures will influence rates of survivors with poor neurological status. Currently, withdrawal of care in comatose patients after cardiac arrest is strongly forbidden by law in Korea. However, a new legislation on allowing withdrawal of care will come into effect since early 2018 in Korea. The investigators aim to determine 1) long-term neurological outcomes in patients who developed IHCA, 2) whether early neurological status can predict late neurological status after IHCA, and 3) whether the proportion of IHCA survivors with good neurological outcomes will change since implementation of new legislation on withdrawal of care.

NCT ID: NCT03000829 Completed - Cardiac Arrest Clinical Trials

Code Blue Outcomes & Process Improvement Through Leadership Optimization Using Teleintensivists-Simulation

COPILOT-Sim
Start date: December 2016
Phase: N/A
Study type: Interventional

This multicenter randomized trial will employ in-situ cardiac arrest simulations ("mock codes") to test whether using telemedicine technology to add an intensive care physician as the "copilot" for cardiac arrest resuscitation teams influences chest compression quality, resuscitation protocol adherence, team function, and provider experience.

NCT ID: NCT02998749 Completed - Clinical trials for Cardiac Arrest With Successful Resuscitation

Gasping Improves Long-term Survival After Out-of-hospital Cardiac Arrest

Start date: July 2013
Phase: N/A
Study type: Observational

The aim of our retrospective clinical study was to examine the association between agonal breathing, return of spontaneous circulation (ROSC), and long-term survival. A secondary aim was to examine role of basic life support (BLS) and response time. Our hypothesis is that agonal breathing has positive effects on both primary and secondary endpoints.

NCT ID: NCT02992873 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

The Scandinavian AED and Mobile Bystander Activation Trial

SAMBA
Start date: December 1, 2018
Phase: N/A
Study type: Interventional

Sudden cardiac death is a major health problem in the western world. In Europe alone nearly 300 000 patients are affected annually. The majority of victims suffering from an Out-of-Hospital Cardiac Arrest (OHCA have an initial cardiac rhythm that can be treated by means of defibrillation. In most emergency medical systems (EMS) time to defibrillation is too long and survival averages 10 %.However, when laymen operated Automated External Defibrillators (AEDs) are used within the first minutes, 7 out of 10 may survive. The aim of "The Scandinavian AED and Mobile Bystander Activation" (SAMBA) trial is to evaluate if a Mobile Phone Positioning system and a smartphone application will increase the proportions of patients with an attached Automated External Defibrillator (AED) before arrival of the Emergence Medical System (EMS). Mobile phone technology and a smartphone application will be used identify and recruit nearby CPR-trained lay people and automated external defibrillators (AEDs) to patients suffering out-of-hospital cardiac arrest (OHCA). The system is currently running in Stockholm Sweden and in the Gothenburg region.

NCT ID: NCT02987088 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

Phase 1 Clinical Trial of Sodium Nitrite for Out of Hospital Cardiac Arrest

Start date: December 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the optimal dose of sodium nitrate administered during resuscitation to achieve a plasma level of 10 μM by hospital arrival. Pharmacokinetic modeling from human cardiac arrest studies suggest that a single 25 mg IV dose of sodium nitrite will achieve the optimal (based on preclinical studies) neuroprotective plasma levels of 10 μM. In this phase-1 open-label dose finding study in 100 patients, we will determine whether 25 mg IV administered during resuscitation will achieve plasma nitrite levels of at least 10 μM by hospital arrival. Dose adjustments, either decreasing or increasing, will be made if necessary permitting us to determine the optimal nitrite dose needed to achieve the 10 μM plasma target. Safety data will also be collected

NCT ID: NCT02973243 Completed - Clinical trials for Myocardial Infarction

The Vital Signs to Identify, Target, and Assess Level (VITAL) Care Study III

Start date: October 5, 2016
Phase: N/A
Study type: Observational

To evaluate the effect of automated recording on frequency of recorded scores, number of automated notifications and serious events.

NCT ID: NCT02963298 Completed - Clinical trials for Reperfusion Syndrome

CRRT for Glutamate Elimination After Cardiac Arrest

GCRRT
Start date: October 2016
Phase: N/A
Study type: Interventional

Glutamate is known to be a mediator for apoptosis after brain hypoxia e.g. due to cardiac arrest. This pilot trial evaluates the possibility of elimination of Glutamate by CRRT after cardiac arrest.

NCT ID: NCT02940964 Completed - Cardiac Arrest Clinical Trials

Evaluation of Culture-specific Popular Music as a Mental Metronome for Cardiopulmonary Resuscitation

COMSCPR
Start date: October 17, 2016
Phase: N/A
Study type: Interventional

Abstract Introduction Bystander cardiopulmonary resuscitation (CPR) can more than double the patient's chance of survival in Out-of-hospital cardiac arrest (OHCA). In Singapore, bystander CPR rate was low. Recent studies have proposed and validated the use of popular songs as aids in performing CPR. These songs may not be widely known when applied to a different population, and further, may lose popularity over time. "Count on me Singapore" (COMS) is believed to be known to over 90% of the Singapore population. Pilot data indicated that CPR performed using COMS as a mental metronome (COMSCPR) can achieve guideline-compliant rate of chest compression with lower fatigue level than CPR guided by the conventional "one-and-two-three-and" (Standard CPR). The investigators hypothesize that COMSCPR is non-inferior to Standard CPR in achieving guideline-compliant rate of chest compression. Methodology The investigators planned a prospective, randomized, crossover non-inferiority trial comparing COMS CPR and Standard CPR. 80 eligible volunteers will be recruited from a convenience sample of camp personnel from a military training camp. After a 15 minutes familiarization session, they will be randomized into two groups (A and B). Group A will proceed to perform one cycle (two minutes) of Standard CPR, while group B will proceed to perform one cycle of COMS CPR. participants will cross over to perform one cycle of the other method of CPR. After completing this second cycle, a survey form will be administered. The Laerdal SkillReporter will be used to measure the CPR performed. After a 7-14 days interval, participants will be recalled to attend a test scenario. Statistical analysis will be used to compare the two arms.

NCT ID: NCT02934555 Completed - Cardiac Arrest Clinical Trials

Ubiquinol as a Metabolic Resuscitator in Post-Cardiac Arrest

Start date: March 2016
Phase: Phase 2
Study type: Interventional

To study the effects of ubiquinol as a "metabolic resuscitator" in post-cardiac arrest.

NCT ID: NCT02932124 Completed - Clinical trials for Out-of-hospital Cardiac Arrest

Application of Mechanical Cardiopulmonary Resuscitation Devices and Their Value in Out-of-hospital Cardiac Arrest: A Retrospective Analysis of the German Resuscitation Registry

Start date: January 2007
Phase: N/A
Study type: Observational [Patient Registry]

The aim of this study was to analyse a large CPR database, the German Resuscitation Registry, to evaluate potential benefits of mechanical CPR devices over manual CPR in adult cardiac arrest victims. The primary endpoint considered is ROSC.