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Heart Arrest clinical trials

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NCT ID: NCT02032030 Completed - Stroke Clinical Trials

Systematic Assessment and Targeted Improvement of Services Following Yearlong Surgical Outcomes Surveys

SATISFY-SOS
Start date: July 2012
Phase:
Study type: Observational [Patient Registry]

Based on limited published epidemiological data, up to an alarming 1 in 50 surgical inpatients die within 30 postoperative days. Based on our own data from the B-Unaware (NCT00281489) and BAG-RECALL (NCT00682825) clinical trials, 30-day postoperative mortality among high-risk surgical patients is comparable to this at Barnes-Jewish Hospital, and 1-year mortality among high-risk surgical patients may be as high as 10%. Short- and intermediate-term postoperative mortality is therefore a pressing public health concern. Similarly, postoperative major morbidity - including delirium, stroke, myocardial infarction, atrial fibrillation, blood clots, renal dysfunction, wound infection, pneumonia, respiratory failure, loss of functionality, and chronic pain - occurs commonly and affects a substantial proportion of surgical patients, critically ill patients and patients undergoing procedures for chronic pain. Many factors associate strongly and independently with postoperative mortality and major morbidity: patient age, functional status, comorbid medical conditions, and duration and invasiveness of surgery, among others. It is a strategic priority to identify pre- and intraoperative risk factors that are subject to modification.

NCT ID: NCT02011568 Completed - Cardiac Arrest Clinical Trials

Mild Versus Moderate Therapeutic Hypothermia in Out-of-hospital Cardiac Arrest Patients

CAPITALCHILL
Start date: August 2013
Phase: N/A
Study type: Interventional

This trial is currently a single-center, randomized, double-blind investigator initiated prospective clinical trial initiated at the University of Ottawa Heart Institute (UOHI). The plan is to expand the trial shortly as a multi-center project. The patients for this study will be recruited amongst comatose survivors of out-of-hospital cardiac arrest (OHCA). The aim of this study is to determine whether neurologic outcomes at six months are improved with moderate (31 degrees Celsius) versus mild (34 degrees Celsius) therapeutic hypothermia (TH) following return of spontaneous circulation (ROSC) in patients suffering OHCA, with ROSC defined as the resumption of sustained perfusing cardiac activity. The primary outcome will be the proportion of patients experiencing death or a poor neurologic outcome at six months after out of hospital cardiac arrest.

NCT ID: NCT02010151 Completed - Clinical trials for Out of Hospital Cardiac Arrest

Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation

Start date: March 2015
Phase: N/A
Study type: Interventional

The hypothesis of this study is Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation (NAD-CPR) would improve survival of out-of-hospital cardiac arrest (OHCA).

NCT ID: NCT02007499 Unknown status - Cardiac Arrest Clinical Trials

Pre-arrival Instructions Effect on Bystander Cardiopulmonary Resuscitation (CPR).

Start date: January 2009
Phase: N/A
Study type: Observational

The investigators hypothesized that pre-arrival instructions would increase the likelihood of bystanders performing Cardiopulmonary Resuscitation (CPR).

NCT ID: NCT02003001 Recruiting - Clinical trials for Ventricular Tachycardia

Botulinum Toxin Injection to Prevent Ventricular Arrhythmias

Start date: June 2013
Phase: Phase 1
Study type: Interventional

The aim of this prospective non-randomized study was to assess the efficacy and safety of endomyocardial botulinum toxin injection in left ventricle for preventing ventricular arrhythmias.

NCT ID: NCT02002481 Recruiting - Cardiac Arrest Clinical Trials

Comparison of the Quality of CPR by Professional Helpers (Emergency Physicians / Paramedics) During Flights

flights
Start date: December 2013
Phase: N/A
Study type: Interventional

Investigation of the influence of narrowness and unusual circumstances on the CPR-quality

NCT ID: NCT02000505 Recruiting - Cardiac Arrest Clinical Trials

Comparison of the Quality of CPR by Lay Rescuers With and Without Feedback Devices

frequenz
Start date: November 2013
Phase: N/A
Study type: Interventional

Comparison of various methods to improve the quality of CPR

NCT ID: NCT01999036 Recruiting - Clinical trials for Out-of-hospital Cardiac Arrest

Save Hearts in Arizona Registry and Education (SHARE) Project

SHARE
Start date: November 2004
Phase:
Study type: Observational

Evaluation of the impact of bystander CPR, prehospital resuscitation protocols, and hospital post-resuscitation protocols for out-of-hospital cardiac arrest patients in the state of Arizona.

NCT ID: NCT01996020 Completed - Clinical trials for Cardiopulmonary Arrest

Measurement of Cerebral Flow Using Transfontanellar Doppler in Infants Under Cardiopulmonary Bypass

Start date: September 2012
Phase: N/A
Study type: Observational

Transfontanellar Doppler can measure the velocity at both the carotid artery and the anterior cerebral artery during cardiopulmonary bypass in congenital heart disease patients. This study can provide reference value of appropriate cerebral blood flow velocity during pediatric cardiac surgery.

NCT ID: NCT01994772 Completed - Cardiac Arrest Clinical Trials

Therapeutic Hypothermia After Cardiac Arrest in Non Shockable Rhythm

HYPERION
Start date: January 26, 2014
Phase: N/A
Study type: Interventional

Cardiac arrest is at present a major cause of mortality as well as a cause of disability for the surviving victims.In Europe, every year counts as 300,000 cardiac arrests responsible for 250,000 deaths. Thus, less than 20 % of patients discharged home with impaired quality of life associated with symptoms of tiredness, stress, anxiety. The prognosis is related to the initial cardiac rhythm present during the initiation of resuscitation. Recent progress in the improvement of mortality and neurological outcome has been achieved over the last decade thanks to the systematic implementation of a period of targeted temperature control between 32 and 34 ° C in patients who benefited from the realization of at least one electrical external shock. There are theoretical and clinical arguments to think that achieving the same way a period of targeted temperature control between 32 and 34 ° C in patients treated for cardiac arrest with a non- shockable rhythm on arrival can also benefit from this procedure. However other arguments are against this hypothesis including an increase in the risk of infection , worsening of the patient's hemodynamic status with no benefit to him. To answer this question, we conduce a randomized multicenter study testing the potential improvement of neurological outcome through this procedure targeted temperature control between 32.5 and 33.5 ° C in these patients.