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Heart Arrest clinical trials

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NCT ID: NCT01295749 Completed - Cardiac Arrest Clinical Trials

Effects of Laryngeal Tube Ventilation on no Flow Time During Out of Hospital Cardiac Arrest

FLOWERS
Start date: March 2011
Phase: Phase 3
Study type: Interventional

International recommendations stress on the importance of no flow time reduction in cardiac arrest management. In fact, no flow time is an independent factor of morbidity and mortality. In France, cardiac arrests are treated by first responders (including emergency nurses) before the arrival of a mobile intensive care unit. Those first responders use bag-valve-mask for ventilation and therefore practice conventional CPR (30 chest compression / 2 ventilation rhythm). Laryngeal tube is a safe and efficient device in cardiac arrest ventilation. The purpose of our study is to compare the no flow time between two strategies of out of hospital cardiac arrest management by first responders: conventional CPR with bag-valve-mask ventilation vs. compression only CPR with Laryngeal Tube ventilation.

NCT ID: NCT01295424 Completed - Cardiac Arrest Clinical Trials

Epidemiology and Cost-effectiveness of Out-Of-Hospital Cardiac Arrest in Finland

FINNRESUSCI
Start date: March 2010
Phase: N/A
Study type: Observational

Observational study of all out-of-hospital cardiac arrest during 6 months in regional areas of Helsinki University Hospital and Kuopio University Hospital from activation of EMS system until follow up to 6 months of survival.Simultaneous observation of out-of-hospital cardiac arrest primary survivors admitted to all Finnish ICUs.

NCT ID: NCT01292148 Completed - Cardiac Arrest Clinical Trials

Measurement of Core Temperatures During Therapeutic Hypothermia

TH
Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine that the measurements of rectal and bladder temperature are correctly consistent with core temperature by using the pulmonary artery catheter during therapeutic hypothermia; rapid cooling, maintenance, and slow rewarming phase.

NCT ID: NCT01280942 Completed - Septic Shock Clinical Trials

Early Warning System for Clinical Deterioration on General Hospital Wards

Start date: January 2011
Phase: N/A
Study type: Interventional

The goal is to develop a two-tiered monitoring system to improve the care of patients at risk for clinical deterioration on general hospital wards (GHWs) at Barnes-Jewish Hospital (BJH). The investigators hypothesize that the use of an automated early warning system (EWS) that identifies patients at risk of clinical deterioration, with notification of nurses on the GHWs when patients are identified, will reduce the risk of ICU transfer or death within 24 hrs of an alert. As a substudy, the investigators will pilot the use of a wireless pulse oximeter to establish feasibility and to develop algorithms for a real-time event detection system (RDS) in these high-risk patients.

NCT ID: NCT01265316 Completed - Cardiac Arrest Clinical Trials

Measurement of the Quality of Pediatric CPR

PediQ-CPR
Start date: October 2010
Phase: N/A
Study type: Observational

Outcomes for pediatric cardiopulmonary resuscitation (CPR) are suboptimal. CPR quality is directly related to resuscitation outcome, yet numerous deficiencies in CPR quality have been documented in adult studies. While similar deficiencies can be expected in pediatric resuscitation attempts, there is little to no data evaluating the existing quality of CPR performed during resuscitation attempts. Therefore, the objective of this study is to quantitatively evaluate existing CPR quality using a Q-CPR compression sensor manufactured by Philips Medical Systems with technology from Laerdal Medical.

NCT ID: NCT01260441 Completed - Coronary Disease Clinical Trials

An In-Hospital Family Member Cardiopulmonary Resuscitation (CPR) Education Program

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

Each year in the United States, 300,000 people suffer from a Cardiac Arrest (CA), and of them, there is a 90% mortality rate. Out-of-Hospital arrests, in particular, have a 1-5% survival to hospital discharge. High quality CPR is crucial to lowering the mortality rate and increasing survival, yet only 15-30% of out-of-hospital CA victims receive bystander CPR. Studies have shown that prompt administration of CPR dramatically improves outcomes. In a recent study from Switzerland, lay bystander CPR doubled the survival rate at one month. Our study will look to train family members of at-risk cardiac patients in the skills of CPR through the American Heart Association's (AHA) CPR Anytime Friends and Family Personal Learning Program (CPR Anytime) to see if these family members are able to learn and perform quality CPR in the event that their family member should suffer a cardiac arrest.

NCT ID: NCT01258244 Completed - Clinical trials for Out-of-Hospital Cardiac Arrest

Arizona Prehospital CPR Quality Improvement Project

Start date: December 7, 2010
Phase: N/A
Study type: Observational

The quality of cardiopulmonary resuscitation (CPR) provided to patients with out-of-hospital cardiac arrest (OHCA) is often suboptimal. There now exist monitors/defibrillators that allow for the measurement and real time feedback of the quality of chest compressions and ventilations. In addition to giving the prehospital provider the benefit of real time CPR quality feedback via voice and visual cues, the CPR quality data acquired using these devices can be utilized as part of an on-going quality assurance/quality improvement program. The first objective of the proposed project is to quantify the quality of chest compressions and ventilations provided in the state of Arizona to patients with OHCA and to determine whether the quality of CPR is related to patient outcome from OHCA. A second objective of this project is to determine whether use of audiovisual feedback improves both CPR quality and patient outcome in the pre-hospital setting.

NCT ID: NCT01252316 Completed - Coronary Disease Clinical Trials

Cardiopulmonary Resuscitation (CPR) Dissemination Study Using Nurses and Volunteers

Start date: October 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Each year in the United States, 300,000 people suffer from Cardiac Arrest (CA), and of them there is a 90% mortality rate. Out-of-Hospital arrests in particular have a 1-5% survival to hospital discharge. High quality CPR is crucial to lowering the mortality rate and increasing survival, yet only 15-30% of out-of-hospital CA victims receive bystander CPR. Studies have shown that prompt administration of CPR dramatically improves outcomes. In a recent study from Switzerland, lay bystander CPR doubled the survival rate at one month. Our study will look to train family members of at-risk cardiac patients in the skills of CPR through the American Heart Associations (AHA) CPR Anytime Friends and Family Personal Learning Program (CPR Anytime) to see if these family members are able to learn and perform quality CPR in the event that their family member should suffer a cardiac arrest. The unique feature of the CPR Anytime training is that it is a low-cost, self-learning, video-based program that can be completed in under 30 minutes, saving the time and expense of traditional CPR training courses. While initial work has proven that teaching CPR in hospital using the VSI kit is feasible, little research has been conducted to make the program sustainable.

NCT ID: NCT01245699 Completed - Cardiac Arrest Clinical Trials

MIHS Emergency Department CPR Quality Improvement Project

Start date: June 9, 2010
Phase: N/A
Study type: Interventional

The investigators will quantify the quality of chest compressions provided in the Emergency Department and determine whether the quality of chest compressions is related to patient outcome. The quality of chest compressions and patient outcomes will be assessed both before and after the introduction of audiovisual feedback in real time.

NCT ID: NCT01197326 Completed - Sepsis Clinical Trials

The Prevention of Failure to Rescue Using Early Warning Scoring

VitalCare
Start date: August 2009
Phase: N/A
Study type: Observational

The purpose of this study is to assess if, compared with standard paper-based systems, an automated Early Warning System (EWS) resident in a spot check patient monitor, can help to identify deteriorating patients.