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Death, Sudden clinical trials

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NCT ID: NCT01422174 Withdrawn - Clinical trials for Myocardial Infarction

Clinical Registry on Sudden Death Primary Prevention at Latin America

ESCAPE-ICD
Start date: March 2012
Phase: N/A
Study type: Observational

INTRODUCTION: Sudden cardiac death is one of the most important reasons of death at industrialized countries. Despite its importance, nowadays Clinical Guidelines are not as extended as expected, with respect to indications for primary prevention defibrillator implantation, following MADIT II and MUSTT criteria, especially at Latin American countries. OBJECTIVES: This Project is designed with the purpose of providing tools to help spreading primary prevention by the means of clinical evidence on real risk of death in this group of patients. REGISTRY DESIGN: - retrospective (at stage 1); prospective (at stage 2) - multi-center (minimum 25-30 centres) - international (Argentina, Brazil, Colombia, Chile, Mexico and Venezuela) - non randomized. - Sample size: at screening about 12.500 patients and 962 patients at treatment stage REGISTRY DEVICES: CE marked (Conformité Européenne) single-chamber, dual-chamber or CRT (Cardiac Resynchronization Therapy) implantable cardiac defibrillator (ICD).

NCT ID: NCT01412502 Terminated - Clinical trials for Stress Disorders, Post-Traumatic

Post Traumatic Stress Among Relatives of Brain-dead, Withdrawal of Life Support, and Sudden Death Patients

Start date: June 15, 2012
Phase: N/A
Study type: Observational

This study concerns the nearest relatives of patients who have passed away within 3 days of admission to an ICU due to: (1) brain death with multiple organ donation +/- tissues or (2) death via limitation and / or cessation of active treatment (LATA) without brain death or (3) sudden death of a previously healthy patient (no physical or mental limitations; MacCabe score = 0) within 3 days of admission to ICU without LATA nor brain death. Our primary objective is to determine the proportion of nearest relatives at risk for post traumatic stress disorder as defined by an Impact of Event Scale score greater than 37, and to compare this factor between the three above-mentioned groups.

NCT ID: NCT01326624 Completed - Heart Failure Clinical Trials

Study of the Wearable Defibrillator in Heart-Failure Patients

SWIFT
Start date: March 2011
Phase: N/A
Study type: Observational

The purpose of the study is to evaluate the safety and efficacy of wearable defibrillator use in patients with left ventricular dysfunction or advanced heart failure symptoms, who have a high-risk for sudden cardiac death but are either not eligible for an implantable defibrillator under current guidelines or are not able to receive the device due to their condition.

NCT ID: NCT01321918 Terminated - Clinical trials for Extra-hospital Sudden Death

Register and DNA Bank of Adult Extra-hospital Sudden Death (Protocol FASTER)

Start date: June 2007
Phase: N/A
Study type: Interventional

The main objective of this study is the formation of a DNA bank to realise a case-control genetic study designed to identify sequence variations in DNA that predispose to sudden cardiac death in adults. The secondary objective of this study is the creation of a register for epidemiological surveillance of adult extra-hospital sudden death.

NCT ID: NCT01214460 Completed - Clinical trials for Death, Sudden,Cardiac

Impact of Medical Emergency Team and EMS in Tampere University Hospital

Start date: January 2010
Phase:
Study type: Observational

Patients in general wards have abnormal physical values preceding in-hospital cardiac arrest or a transfer to intensive care unit (ICU). The purpose of Medical Emergency Team (MET) or EMS is to interfere early enough in deteriorating patient status to prevent adverse outcomes like cardiac arrest or transfer to intensive care unit. The aims of this study are to record and analyze the effects of EMS and department of emergency and both afferent and efferent limbs of MET activity in Finnish tertiary Hospital.

NCT ID: NCT01185756 Active, not recruiting - Heart Failure Clinical Trials

MIBG Scintigraphy as a Tool for Selecting Patients Requiring Implantable Cardioverter Defibrillator (ICD)

MISTIC
Start date: September 2010
Phase: N/A
Study type: Interventional

The aim of the study is to assess the cardiac innervation in patients with heart failure to better select candidates for an implantable cardioverter defibrillator. Cardiac innervation will be assessed using an imaging agent administered intravenously.

NCT ID: NCT01013311 Completed - Cardiomyopathy Clinical Trials

Implantable Cardiac Defibrillators for the Prevention of Sudden Death in Patients With Cardiac Sarcoidosis

Start date: November 2009
Phase:
Study type: Observational

The purpose of this study is to identify patients with cardiac sarcoidosis who may be at risk for sudden death.

NCT ID: NCT00920244 Completed - Heart Arrest Clinical Trials

In-hospital Cardiac Arrest - Dynamics and State Transitions

Start date: August 2009
Phase:
Study type: Observational

The purpose of this study is to analyse transitions in cardiac rhythm and hemodynamic variables during resuscitation of patients with in-hospital cardiac arrest.

NCT ID: NCT00859300 Completed - Clinical trials for Myocardial Infarction

MAP-IDM: Identification of Molecular Markers of Sudden Death at the Acute Phase of Myocardial Infarction

MAP-IDM
Start date: December 2007
Phase: N/A
Study type: Observational

We propose a comparative case-control study on the 2 following groups of patients: - Cases: 500 patients with ventricular fibrillation at the acute phase of myocardial infarct, - Controls: 500 patients without ventricular fibrillation at the acute phase of myocardial infarct. The primary endpoint in this study is the correlation phenotype/genotype of sudden death at the acute phase of myocardial infarct. The first phase of the study, including patients' recruitment, clinical and biological data collection, will last 82 months. The second phase will concern the genotype/phenotype analysis and the identification of polymorphisms associated with a sudden death risk after a myocardial infarction. This study will allow a better knowledge of the mechanisms of sudden death and the identification of new risk markers.

NCT ID: NCT00741728 Recruiting - Clinical trials for Cardiovascular Disease

Heart Rate, Baroreflex Sensitivity and Cardiovascular Morbidity and Mortality in the Population

PPSIII
Start date: June 2008
Phase: N/A
Study type: Observational

The aim of the present PPS3 study is (1) to assess the determinants of the regulation of heart rate and blood pressure variations and carotid properties (under different physiologic stimulations) and (2) to evaluate the respective contribution of heart rate, blood pressure variations and carotid properties to cardiovascular morbidity and mortality including sudden death during 10 years at least in healthy considered subjects.