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Heart Arrest clinical trials

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NCT ID: NCT01560338 Completed - Cardiac Arrest Clinical Trials

Hypothermia's Impact on Pharmacology

HIP
Start date: March 2012
Phase:
Study type: Observational

The purpose of the study will help us understand the complex interaction between hypothermia (cooling) and pharmacogenetics (how specific genes effect how drugs are handled), and their impact on how routinely given sedation drug are broken down and used by the body when given to children after cardiac arrest (when heart stops pumping blood) and are critically ill.

NCT ID: NCT01531426 Completed - Cardiac Arrest Clinical Trials

Cerebral Oxygenation in Cardiac Arrest and Hypothermia

CoCaHYp
Start date: January 2012
Phase: N/A
Study type: Observational

Data indicate that neurological prognostication is difficult after cardiac arrest if mild therapeutic hypothermia is part of the post resuscitation care. Cerebral oxygenation detected by near-infrared spectroscopy, could be a new, non-invasive index marker for outcome assessment after cardiac arrest. The investigators hypothesize that cardiac arrest survivors with a continuously low cerebral oxygenation index have a poor prognosis.

NCT ID: NCT01528475 Completed - Clinical trials for Out of Hospital Cardiac Arrest

Initiation of Cooling by EMS to Promote Adoption of In-hospital Hypothermia in Cardiac Arrest Survivors

Start date: July 2012
Phase: N/A
Study type: Interventional

This is a large pragmatic, randomized controlled trial comparing pre-hospital initiation of therapeutic hypothermia by Emergency Medical Services (EMS) providers to conventional post-resuscitation care. The goal of this trial is to increase the proportion of cardiac arrest patients that are appropriately treated in-hospital with therapeutic hypothermia to reach the target body temperature within 6 hours of hospital arrival. The investigators believe that EMS-initiation of cooling will be a powerful reminder to in-hospital clinicians to continue therapeutic hypothermia, and will lead to care improvements across a health system.

NCT ID: NCT01509040 Completed - Cardiac Arrest Clinical Trials

Washington Study of Hemofiltration After Out-of-Hospital Cardiac Arrest

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the feasibility of hemofiltration in patients resuscitated from cardiac arrest. Cardiac arrest is the loss of mechanical activity of the heart including the loss of detectable pulse, or spontaneous breathing. When heart function is restored, the cells of the body release molecules into the blood that cause inflammation, unstable blood pressure, organ dysfunction and death. Hemofiltration is a technique of washing the blood to remove fluid and molecules from it. Hemofiltration is a proven therapy for renal failure, but is considered investigational for treatment after resuscitation from cardiac arrest. Some experts believe that hemofiltration after heart function is restored can remove inflammation from the blood, maintain blood pressure and organ function. Others believe that intravenous fluid and medications are sufficient to maintain blood pressure and organ function. Since the inflammation that occurs after restoration of heart function lasts, the investigators continue hemofiltration for up to 48 hours. Whether hemofiltration or intravenous fluids and medications is better is not known. The investigators are checking if they can wash the blood of patients resuscitated from cardiac arrest before the investigators can begin a large randomized trial to test whether hemofiltration improves their outcome. The investigators are testing this by randomly allocating patients resuscitated from cardiac arrest to receive low volume hemofiltration, high volume hemofiltration, or intravenous fluids and medications alone. The null hypotheses are that less than 80% of eligible patients will be enrolled, and that less than 80% of enrolled patients will undergo low-volume or high-volume hemofiltration (HF) for at least 80% of 48 hours.

NCT ID: NCT01502111 Completed - Trauma Clinical Trials

Airway Management Study in Physician Manned Helicopter Emergency Medical Services

AIRPORT
Start date: January 2012
Phase: N/A
Study type: Observational

An international airway management expert group has recently developed an Utstein-style template for uniform reporting of data from prehospital advanced airway management. Implementing and validating the template will result in a high quality dataset and allow for research cooperation and comparison of airway management practice between EMS systems, and across different patient populations. Such a dataset will hopefully contribute to new knowledge in the field of prehospital advanced airway management.

NCT ID: NCT01472458 Completed - Cardiac Arrest Clinical Trials

Premature Termination of Resuscitation in Survivors of Cardiac Arrest

PremaTOR
Start date: November 2011
Phase: N/A
Study type: Interventional

The study Premature Termination of Resuscitation in Survivors of Cardiac Arrest focuses on using innovative knowledge translation strategies to improve appropriate neuroprognostication for survivors of cardiac arrest and prevent premature termination of life sustaining therapies. This is important because any early gains achieved during resuscitation will be nullified if clinicians terminate life-sustaining therapies prematurely based on inadequate prognostic information. An effective translation strategy for neuroprognostication will result in improved physician adherence to evidence-based medicine and an increase in the proportion of patients surviving to achieve a good neurological outcome following cardiac arrest.

NCT ID: NCT01452867 Completed - Clinical trials for Cardiopulmonary Arrest

Comparison of Ventilation With Bag-Valve-Mask, Laryngeal Tube S-D and Laryngeal Mask Airway Supreme

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

Inexperienced rescuers may encounter severe problems in an unconscious patient in opening and maintaining an upper airway patent. Gaining evidence which ventilation technique may be most efficient and safe is of utmost importance to potentially improve outcome during cardiopulmonary resuscitation.

NCT ID: NCT01446471 Completed - Cardiac Arrest Clinical Trials

REASON 1 Trial: Sonography in Cardiac Arrest

Start date: January 2010
Phase: N/A
Study type: Observational

The aim of this study is to investigate the predictive value of the presence or absence of cardiac activity by bedside ultrasound during cardiac arrest. The investigators anticipate based on previous research that patients who suffer a cardiac arrest and have cardiac activity on bedside ultrasound will have a greater chance of surviving to hospital admission. The investigators hypothesis is that the mortality rate in patients in cardiac arrest with no cardiac activity by ultrasound will have a mortality rate of 100%.

NCT ID: NCT01446354 Completed - Cardiac Arrest Clinical Trials

Goal-orientated Coagulation Management in Hypothermic Cardiac Arrest Surgery

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

Cardiac surgery including hypothermic cardiac arrest (HCA) commonly involves perioperative transfusion of allogeneic blood products which is associated with increased morbidity and mortality. In this retrospective analysis, the investigator aimed to evaluate the effect of a thromboelastometry-guided treatment algorithm promoting fibrinogen concentrate as first line hemostatic agent on the perioperative use of allogeneic blood products.

NCT ID: NCT01419106 Completed - Hypotension Clinical Trials

Sonography in Hypotension and Cardiac Arrest in the Emergency Department.

SHoC-ED
Start date: August 2011
Phase: N/A
Study type: Interventional

This study is designed to determine if there is any relationship between performing an abdominal ultrasound on patients who present with hypotension and their clinical outcomes (as measured by 7, 30 day and discharge mortality).