Clinical Trials Logo

Heart Arrest clinical trials

View clinical trials related to Heart Arrest.

Filter by:
  • Active, not recruiting  
  • « Prev · Page 5

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: NCT01239420 Active, not recruiting - Cardiac Arrest Clinical Trials

Norwegian Cardio-Respiratory Arrest Study

NORCAST
Start date: September 2010
Phase:
Study type: Observational

The purpose of this study is to evaluate the use of combined clinical-neurological, neurophysiologic, neuroradiological and biochemical markers in prognostication after cardio- and/or respiratory arrest.

NCT ID: NCT00998140 Active, not recruiting - Clinical trials for Cardiopulmonary Arrest Outcome

Optimizing Resuscitation After Cardiac Arrest in the Community

Start date: March 2009
Phase:
Study type: Observational

Resuscitative efforts have been shown to be unsuccessful in most cases of out-of-hospital cardiac arrest (OHCA), and survivors who do recover cardiac function often sustain severe hypoxic brain damage. Time to efficacious care is a primary determinant of disability-free survival. In the Jerusalem district, only 9% of OHCA patients present with ventricular tachycardia/ventricular fibrillation (VT/VF) as the primary rhythm, whereas 77% present with asystole; this seems primarily to be the result of long collapse-to-arrival times. Nevertheless, overly zealous resuscitation is undertaken in a high proportion of arrests with a futile prognosis, leading to excessive costs. Study hypotheses: 1. Subpopulations for whom intervention is futile/counter-productive are identifiable 2. Substantial waste of resources can be avoided 3. Optimization of emergency medical services (EMS) reorganization without adding resources is an achievable goal

NCT ID: NCT00814814 Active, not recruiting - Clinical trials for Cardiopulmonary Arrest Outcome

Protein S100 Beta as a Predictor of Resuscitation Outcome

Start date: February 2008
Phase:
Study type: Observational

Management of cardiac arrest is complicated by the lack of a readily available tool identifying individuals who are likely to be successfully resuscitated. S100 beta is a protein that originates in the astroglial cells of the brain, and NSE (Neuron Specific Enolase) is another protein that originates in the neurons themselves. In the laboratory, the concentration of these proteins correlate with evidence of brain damage after head trauma, stroke and exposure to low levels of oxygen. The concentration of these proteins in the blood of human survivors of cardiopulmonary resuscitation in humans is much higher than in patients who were resuscitated but did not survive. However, it is still unclear whether survivors from cardiopulmonary resuscitation have higher levels of these proteins in their blood if they survive with neurological injury secondary to the arrest and resuscitation. Hypothesis: In humans, the blood concentrations of protein S100 beta and NSE during and after resuscitation can predict who will die despite cardiopulmonary resuscitation and who will survive with neurological injury secondary to the arrest and resuscitation.

NCT ID: NCT00661128 Active, not recruiting - Clinical trials for Death, Sudden, Cardiac

Genomics of Sudden Cardiac Arrest

GenSCA
Start date: September 2007
Phase:
Study type: Observational

Sudden cardiac arrest (SCA) is a sudden, unexpected loss of heart function. It is a leading cause of death, and more than 400,000 people in the United States die each year as a result of SCA. This study will analyze genetic samples of people who have experienced SCA and people who have not experienced SCA to determine if there is a genetic basis for SCA.