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Heart Arrest clinical trials

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NCT ID: NCT01413399 Completed - Clinical trials for Out-of-Hospital Cardiac Arrest

A Pilot Study of Intra-arrest Therapeutic Hypothermia in Patients Suffering Non-Traumatic Out of Hospital Cardiac Arrest

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

The objective of this study will be to assess the frequency of return of spontaneous circulation (ROSC), survival to admission, survival to discharge from the hospital, and neurologic function at time of discharge from the hospital among patients experiencing out of hospital cardiac arrest randomized to receive either intra-arrest induction of therapeutic hypothermia (IATH) or post-arrest therapeutic hypothermia (TH).

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: NCT01400373 Completed - Clinical trials for Out-of-hospital Cardiac Arrest

Prehospital Resuscitation Intra Nasal Cooling Effectiveness Survival Study

PRINCESS
Start date: July 6, 2010
Phase: Phase 2
Study type: Interventional

Promising result of intra-arrest cooling on neurological intact survival in cardiac arrest patients has recently been published in the PRINCE-study in Circulation 2010. The main purpose of this study is to determine whether prehospital intra-nasal cooling initiated during resuscitation, in addition to systemic cooling at hospital, increases neurological intact survival measured as cerebral performance category score (CPC-score)at 90 days in witnessed cardiac arrests outside hospital.

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: NCT01390675 Recruiting - Heart Failure Clinical Trials

Anesthesia for Catheter Aortic Valve ImplantATIOn Registry

AVIATOR
Start date: June 2011
Phase:
Study type: Observational

In modern cardiac surgery and cardiology Transcatheter Aortic Valve Implantation (TAVI) is an emerging procedure for high-risk patients that are assumed to be otherwise inoperable. The investigators want to evaluate the specific intraoperative anesthesiologic characteristics cardiac anesthesiologists have to face during these procedures.

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: NCT01377337 Not yet recruiting - Clinical trials for Sudden Cardiac Arrest

Sodium Bicarbonate in Cardiopulmonary Resuscitation

SB CAT
Start date: December 2011
Phase: Phase 4
Study type: Interventional

Out-of-hospital cardiac arrests (OHCA) account for over 60% of deaths from coronary artery disease. The annual incidence of OHCA treated by Emergency Medical Systems (EMS) is 41-89 per 100,000 population. Outcome of OHCA and cardiopulmonary resuscitation (CPR) is very poor: Less than 1/3 of the victims regain spontaneous circulation (ROSC), 40-60% of those achieving ROSC suffer significant neurological disability due to brain hypoxia and only 1.7-6.4% are discharged from the hospital. In order to minimize hypoxia time, the primary goal of CPR is to achieve return of spontaneous circulation (ROSC) as fast as possible. Metabolic (lactic) acidosis develops rapidly during CA and is considered detrimental to CPR outcome. Sodium bicarbonate (SB), a generic, commonly used acid buffer, was subjected only to a single, small, prospective controlled trial that found a trend towards improved outcome in prolonged OHCA and CPR. Another study indicated that EMS's that used SB early and often during CPR had significantly higher ROSC rates and better long-term outcome compared with EMS's that used SB more seldom and administered it late in the course of CPR. Aim of the Study: To determine whether early administration of SB during OHCA and CPR improves short-term CPR outcome.

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: NCT01372748 Completed - Clinical trials for Out of Hospital Cardiac Arrest

Continuous Chest Compressions vs AHA Standard CPR of 30:2

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

The primary aim of the trial is to compare survival to hospital discharge after continuous chest compressions (CCC) versus standard American Heart Association (AHA) recommended cardiopulmonary resuscitation (CPR) with interrupted chest compressions (ICC) in patients with out-of-hospital cardiac arrest (OOHCA). The primary null hypothesis will be that the rate of survival to hospital discharge is not affected by use of continuous compressions with passive or positive pressure ventilation (intervention group) versus CPR with compressions interrupted for ventilation at a ratio of 30:2 (control group).

NCT ID: NCT01369732 Completed - Clinical trials for Dissection of Thoracic Aorta

Prevention of Acute Kidney Injury by Erythropoietin in Thoracic Aorta Surgery With Hypothermic Cardiac Arrest

Start date: May 2011
Phase: Phase 4
Study type: Interventional

During thoracic aortic surgery, hypothermic cardiac arrest causes aortic ischemia and reperfusion (IR) periods, respectively. Aortic ischemia results in an ischemic insult to the lower extremities and successive reperfusion results in injury to remote organs, including kidneys. So, there has been considerable interest in the development of therapeutic strategies aimed at attenuating IR injury. One such group of agents that are attracting interest due to their potential protective effects on vascular endothelium is the erythropoietin. However, the effect of erythropoietin on renal injury induced by aortic IR in humane has not been fully clarified. Therefore, the purpose of this study is to determine whether the prophylactic administration of erythropoietin reduce the incidence of acute kidney injury (AKI) in patients undergoing thoracic aorta surgery with hypothermic cardiac arrest. The investigators administrate the erythropoietin single bolus (500 IU/kg intravenously) 30 min before the commencement of ischemia. The differences between the control and study groups are observed by clinical indicators such as serum creatinine, TNF-α, NGAL.