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Heart Arrest clinical trials

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NCT ID: NCT00754481 Completed - Cardiac Arrest Clinical Trials

Hypothermia for Cardiac Arrest in Paediatrics

Start date: January 2005
Phase: Phase 2
Study type: Interventional

The investigators hypothesized that, following cardiac arrest in pediatric patients, hypothermia therapy will improve the proportion of patients with a good functional outcome compared to a normothermic control group.

NCT ID: NCT00729794 Completed - Cardiac Arrest Clinical Trials

Vasopressin, Epinephrine, and Steroids for Cardiac Arrest

VSE-2
Start date: September 2008
Phase: Phase 3
Study type: Interventional

The simultaneous activation of adrenergic and vasopressin receptors, in conjunction with a potential steroid-mediated enhancement of the vascular reactivity to epinephrine may have beneficial effects in patients with cardiac arrest. This hypothesis is supported by the single-center results of NCT 00411879. The investigators intend to either refute or provide definitive evidence supporting this hypothesis (and its generalizability) by conducting the present multicenter, randomized, controlled clinical trial of in hospital cardiac arrest.

NCT ID: NCT00719498 Completed - Cardiac Arrest Clinical Trials

Effect of Early High-dose Epoetin Alfa During Cardiac Arrest (Pilot Study)

Start date: November 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the possible neuroprotective effect of early high dose erythropoietin alpha after out of hospital cardiac arrest (OHCA).

NCT ID: NCT00683683 Completed - Cardiac Arrest Clinical Trials

The Strategies for Post Arrest Resuscitation and Care Network

SPARC
Start date: April 2008
Phase: N/A
Study type: Interventional

Background: One of the 2010 Impact Goals of the Emergency Cardiac Care (ECC) Committee of the American Heart Association is to double survival from cardiac arrest. Currently, approximately 60% of adults and 50% of paediatric patients that regain spontaneous circulation following cardiac arrest die before leaving the hospital. A key piece of the "chain of survival" is this fifth link; the care of patients post-arrest. Although there are several modalities recommended for post arrest care, therapeutic hypothermia is the only in-hospital therapy that has been demonstrated in randomized clinical trials to improve patient outcome after cardiac arrest. Despite the strong evidence for its efficacy and the apparent simplicity of this intervention, recent surveys show that hypothermia is delivered inconsistently, incompletely, and with undue delay in hospitals receiving resuscitated patients; only 26% of physicians and 26% of hospitals regularly institute a hypothermia protocol. Primary Objective: To design and apply a knowledge translation program for the 2005 AHA guideline on hypothermia post cardiac arrest and enable effective implementation of hypothermia in 100% of eligible OHCA patients. The integration of two robust data collection systems, which include both pre-hospital and in-hospital indicators, will give complete process of care and clinical outcome information for all cardiac arrest patients. Primary Endpoint: the proportion of eligible out of hospital cardiac arrest patients cooled to 32-34°C within 6 hours of ED arrival. Study Design: This project will be implemented through an established research collaborative of 43 hospitals in southern Ontario currently participating in the Toronto site of the Resuscitation Outcomes Consortium. A stepped wedge study design will be employed, whereby the intervention will be rolled-out sequentially to the participating hospitals over a number of time periods as sites reach pre-defined benchmarks. The multifaceted KT strategy will include 1) local multidisciplinary champions in ED, ICU, and Cardiology 2) A simple protocol for application of hypothermia, tailored to local needs and policy; 3) Identification of perceived and actual barriers to knowledge use; 4) Development of an implementation tool kit and 5) Providing timely feedback on benchmarks for hypothermia and outcomes

NCT ID: NCT00676598 Completed - Cardiac Arrest Clinical Trials

A Prospective Analysis of the Effect of Therapeutic Hypothermia After Cardiac Arrest

Start date: January 2007
Phase: N/A
Study type: Observational

Therapeutic hypothermia has been shown to improve survival and neurologic outcome in patients resuscitated after ventricular fibrillation arrest. Few studies have examined whether therapeutic hypothermia is effective outside the research setting, or with other presenting rhythms. Our institution, a large community teaching hospital, instituted a therapeutic hypothermia protocol in November 2006 for all resuscitated cardiac arrest patients. The investigators seek to determine the mortality rate of our protocol and compare our complication rates with those of previously published studies.

NCT ID: NCT00676585 Completed - Cardiac Arrest Clinical Trials

Corticosteroid Therapy in Refractory Shock Following Cardiac Arrest

Start date: October 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The major goal of this project is to determine whether the use of physiologic doses of corticosteroids will decrease time to shock reversal, alters the inflammatory cascade, and alters microcirculatory flow in post-cardiac arrest patients.

NCT ID: NCT00665288 Completed - Cardiac Arrest Clinical Trials

Survey of Attitudes and Factors Associated With CPR in an Older Population

Start date: January 2008
Phase:
Study type: Observational

The goal of this study is to conduct a survey to better understand the factors associated with undertaking cardiopulmonary resuscitation (CPR) training and performing CPR in an emergency situation.

NCT ID: NCT00664443 Completed - Cardiac Arrest Clinical Trials

Effectiveness of Dispatch-Assisted Cardiopulmonary Resuscitation (CPR) Instructions

Start date: July 2007
Phase: Phase 1
Study type: Observational

The overall goal of this study is to better understand the factors leading to successful dispatch-assisted CPR instructions and to ultimately save the lives of more cardiac arrest patients. Specific objectives are to: 1) Determine the ability of 9-1-1 dispatchers to make the diagnosis of cardiac arrest over the phone; 2) Quantify the frequency and impact of perceived agonal breathing on cardiac arrest diagnosis; 3) Measure the frequency with which dispatch-assisted CPR instructions can be successfully completed in out-of-hospital cardiac arrest cases; and 4) Measure the impact of dispatch-assisted CPR instructions on bystander CPR and survival rates for out-of-hospital cardiac arrest.

NCT ID: NCT00650962 Completed - Cardiac Arrest Clinical Trials

Pre-shock Cardiopulmonary Resuscitation to Patients With Out-of-hospital Resuscitation, A Randomised Clinical Trial

CPR
Start date: February 2008
Phase: N/A
Study type: Interventional

1. Pre-shock cardiopulmonary resuscitation might benefit the survival of out-of-hospital cardiac patients with ventricular fibrillation / ventricular tachycardia in a post-hoc analysis of a prehospital trial conducted in Europe (L.Wik,2002). However, it's effectiveness in the Asian countries, where most firstly recorded rhythm in out-of-hospital cardiac arrests patients were asystole/pulseless electric activity rather than ventricular fibrillation / ventricular tachycardia, were not explored yet. 2. This trial was designed to exam if pre-shock cardiopulmonary resuscitation by emergency medical technicians improves the outcome of all out-of-hospital cardiac arrest patients in an Asian metropolitan city.

NCT ID: NCT00644722 Completed - Cardiac Arrest Clinical Trials

Out-of-Hospital Intubation With Metal Single Use Laryngoscope Blades

LAMETA
Start date: April 2008
Phase: Phase 4
Study type: Interventional

New single use laryngoscope metal blades are available for intubation. This type of blade is safer than the reusable ones concerning the interhuman cross infection risk. No clinical studies have compared the two types of blades in the emergency context. The primary aim of this study is to demonstrate that single use blades are as efficient as the reusable ones concerning intubation conditions.