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Cardiac Arrest clinical trials

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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: NCT01455662 Recruiting - Cardiac Arrest Clinical Trials

Relationship Between Tissue Markes in Patients With Post Cardio Respiratory Syndrome

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

There is a correlation between hospital mortality and changes in markers of tissue perfusion, lactate, and venous oxygen saturation and carbon dioxide gradient.

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: NCT01431326 Completed - Hypertension Clinical Trials

Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care

PTN_POPS
Start date: November 2011
Phase:
Study type: Observational

Understudied drugs will be administered to children per standard of care as prescribed by their treating caregiver and only biological sample collection during the time of drug administration will be involved. A total of approximately 7000 children aged <21 years who are receiving these drugs for standard of care will be enrolled and will be followed for up a maximum of 90 days. The goal of this study is to characterize the pharmacokinetics of understudied drugs for which specific dosing recommendations and safety data are lacking. The prescribing of drugs to children will not be part of this protocol. Taking advantage of procedures done as part of routine medical care (i.e. blood draws) this study will serve as a tool to better understand drug exposure in children receiving these drugs per standard of care. The data collected through this initiative will also provide valuable pharmacokinetic and dosing information of drugs in different pediatric age groups as well as special pediatric populations (i.e. obese).

NCT ID: NCT01401647 Active, not recruiting - Cardiac Arrest Clinical Trials

Amiodarone, Lidocaine or Neither for Out-Of-Hospital Cardiac Arrest Due to Ventricular Fibrillation or Tachycardia

ALPS
Start date: May 2012
Phase: Phase 3
Study type: Interventional

The primary objective of the trial is to determine if survival to hospital discharge is improved with early therapeutic administration of a new Captisol-Enabled formulation of IV amiodarone (Nexterone-PM101) compared to placebo.

NCT ID: NCT01397656 Completed - Cardiac Arrest Clinical Trials

Bystander Fatigue and CPR Quality Using Continuous Compressions Versus 30:2 Compressions to Ventilation

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

STUDY OBJECTIVES The overall goal of this study is to compare bystander fatigue and CPR quality after 5 minutes of continuous chest compressions versus the 2005 30:2 chest compression to ventilation Resuscitation Guidelines, in a population aged 55 or greater. More specifically, the investigators will compare each CPR ratio with regard to: 1. The achieved frequency and depth of chest compressions, and 2. Participant rating of their perceived level of exertion. STUDY HYPOTHESIS In a population aged 55 or greater, the new CPR recommendations will lead to: 1. less frequent and shallower chest compressions over the 5-minute study period; and 2. higher rating of perceived level of exertion when compared to the 2005 30:2 CPR ratio.

NCT ID: NCT01390506 Withdrawn - Cardiac Arrest Clinical Trials

Selenium to Improve Neurological Outcome After Cardiac Arrest

SCPR
Start date: January 2017
Phase: Phase 2
Study type: Interventional

After cardiac arrest and successful resuscitation it can happen that the brain function of a patient is impaired because the brain was without oxygen for a prolonged period of time. Several strategies have been studied to improve brain function after cardiac arrest. Cooling of the patients is routinely used today. The trace element selenium has several biological functions and is important for defense mechanisms against oxidative stress, which occurs after cardiac arrest and successful resuscitation. critically ill patients have low selenium blood levels. Therefore the investigators hypothesize that giving selenium after cardiac arrest and successful resuscitation might improve brain function.

NCT ID: NCT01374061 Withdrawn - Cardiac Arrest Clinical Trials

Pre Hospital Evaluation of Video Laryngoscopy

EVE
Start date: June 2011
Phase: Phase 4
Study type: Interventional

The objective of this work is to compare standard intubation with video laryngoscope (Glide scope Ranger ) in French pre hospital multicentric study.

NCT ID: NCT01362556 Completed - Cardiac Arrest Clinical Trials

Blood Gas Analysis and Buffering In Cardiac Arrest

BABICA
Start date: March 2011
Phase: N/A
Study type: Interventional

The debate over the administration of sodium bicarbonate in cardiac arrest has been going on for several decades, swinging like a pendulum from "first-line drug" to "not indicated" to the recent guidelines advocating "a small bolus under special conditions (metabolic acidosis, intoxication, long-term resuscitation)". A targeted, blood-gas controlled application under optimised ventilation conditions has not yet been evaluated prehospitally. Our preliminary studies have shown that an arterial puncture/line as well as measurement of blood gases is feasible in preclinical conditions. This multicentre trial including 5 centres and 10 physician-staffed emergency systems is designed to compare, in a prospective randomised controlled study, the effect of a calculated dosage of sodium bicarbonate based on the patient´s base deficit and weight, on ROSC (= return of spontaneous circulation) and on the secondary survival of cardiac arrest patients. The null hypothesis is that there is no or negative impact on survival.