Clinical Trials Logo

Heart Arrest clinical trials

View clinical trials related to Heart Arrest.

Filter by:

NCT ID: NCT03889340 Completed - Clinical trials for Cardiac Arrest With Successful Resuscitation

Study of Brain Cools Device in Patients Resuscitated From Cardiac Arrest

Start date: May 1, 2019
Phase:
Study type: Observational

This submission is a pilot in which the new IQool Warming System device will be used to maintain the temperature of adult patients in cardiac arrest within a range of within a range of 32°C to 38.5°C (89.6°F to 101.3°F). The IQool Warming System has received a 510 K Clearance by the FDA.

NCT ID: NCT03881865 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

P25/30 SSEPs and Neurological Prognosis After Cardiac Arrest

Start date: October 8, 2018
Phase:
Study type: Observational

Study Title: Early recorded P25/30 somatosensory evoked potentials are associated with neurologic prognosis of comatose survivors after out of hospital cardiac arrest. Design: Prospective, observational, non-interventional, study - prospective collection of data and interpretation. Analysis of the data and assessment of prognostic value of the P25/30 in critically ill patients post cardiac arrest. Study Aims: To be the first attempt to validate the prognostic potential of early recording [between 24-36 hours post Return Of Spontaneous Circulation] of P25/30 potentials in comatose survivors who are admitted to a British Intensive care unit after out of hospital cardiac arrest and who are not treated by hypothermic targeted temperature management. [Validation of the prognostication significance of P25/30 Somatosensory Evoked Potentials in predicting neurologic outcome in comatose survivors post out of hospital cardiac arrest]. Outcome Measures: Primary Endpoint: Neurologic outcome assessed by Cerebral Performance Category score at hospital discharge. Secondary endpoints: Mortality at hospital discharge and 28 days [which occurs first], comparison of prognostic benefit of N20 and P25/30 based multimodal prognostic models. Population: Comatose survivors, after out of hospital cardiac arrest, treated in Derriford Hospital ICU, Penrose and Pencarrow wards. Eligibility: Adults [>18 years old], out of hospital cardiac arrest, comatose after Return Of Spontaneous Circulation, admission to intensive care Estimated Duration:36 months

NCT ID: NCT03872960 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

A Randomised Trial of Expedited Transfer to a Cardiac Arrest Centre for Non-ST Elevation Out-of-hospital Cardiac Arrest

ARREST
Start date: February 2, 2018
Phase: N/A
Study type: Interventional

The aim of ARREST is to determine the best post-resuscitation care pathway for out of hospital cardiac arrest patients without ST-segment elevation. The investigators propose that changes to emergency management comprising expedited delivery to a specialist heart attack centre with organised post-cardiac arrest care including immediate access to reperfusion therapy will reduce mortality in patients without STE compared to the current standard of care, which comprises protracted pre-hospital management of the patient without definitive care plan and delivery to geographically closest hospital.

NCT ID: NCT03863015 Completed - Clinical trials for Out-Of-Hospital Cardiac Arrest

IL-6 Inhibition for Modulating Inflammation After Cardiac Arrest

IMICA
Start date: March 4, 2019
Phase: Phase 2
Study type: Interventional

Resuscitated cardiac arrest is associated with a systemic inflammatory response that is directly associated with poor prognosis. Inhibition of the IL-6 mediated immune response may potentially inhibit the systemic inflammatory response, potentially improving the prognosis of these severely ill patients.

NCT ID: NCT03849911 Completed - Clinical trials for Neurological Prognosis Cardiac Arrest

EEG and SEP Evaluation for Good and Poor Neurological Prognosis After Cardiac Arrest

ProNeCA
Start date: June 1, 2016
Phase:
Study type: Observational

Hypoxic-Ischemic-encephalopathy (HIE) is a severe and frequent neurological complication of successful cardiopulmonary-resuscitation after cardiac arrest (CA). Prognosticating neurological outcomes in patients with HIE is challenging and recent guidelines suggest a multimodal approach. Only few studies have analyzed the prognostic power of the association between instrumental tests and, in addition, most of them were monocentric, retrospective and evaluating only poor outcome.

NCT ID: NCT03807206 Completed - Clinical trials for Cardiopulmonary Arrest

Resuscitation Outcomes in the Netherlands Flashmob Questionnaire

ROUTINE-F
Start date: January 1, 2019
Phase:
Study type: Observational

The aim of this study is to gain insight in patients' experiences regarding do not resuscitate conversations and decisions. A multicentre flash mob investigation will be conducted in which data will be obtained over the course of two weeks using electronic questionnaires that patients will fill out. General demographic data and a brief quality of life assessment (EQ-5D) will be collected. Whether a DNR converstation has taken place will be noted, along with patients' experiences with this conversation. Lastly the patient will be asked about his/her expectations of survival after cardiopulmonary resuscitation.

NCT ID: NCT03743584 Completed - Clinical trials for Inflammatory Response

Hypothermia After Cardiac Arrest - Effects on Myocardial Function and Inflammatory Response.

IH3
Start date: November 8, 2018
Phase: N/A
Study type: Interventional

The on-going randomized clinical trial TTM2 (Target Hypothermia Versus Targeted Normothermia After Out-of-hospital Cardiac Arrest, NCT02908308) investigates if there is a difference in mortality, neurological function or quality of life in comatose survivors after out-of-hospital cardiac arrest if treated (Group A) at target temperature of 33 oC or (Group B) by avoiding fever during the first 24 h. In this sub study, the effect of different target temperatures on cardiac and circulatory physiology is evaluated by echocardiography and pulmonary artery catheter. Tissue damage after cardiac arrest in part is caused by an activation of different parts of the inflammatory system (reperfusion injury). This study investigates the effect of temperature management on inflammation and the link to the circulatory effects.

NCT ID: NCT03742167 Completed - Respiratory Failure Clinical Trials

Pilot Simulation RCT of Telemedical Support for Paramedics

Start date: December 18, 2018
Phase: N/A
Study type: Interventional

This study evaluates the impact of video communication via telemedicine on the quality of emergency care provided to children by paramedic teams supported by a remote physician in a simulated out-of-hospital setting. Half of the paramedic teams will use a video telemedicine platform for communication with a physician, while the other half will use an audio-only platform.

NCT ID: NCT03733158 Completed - Clinical trials for Endotracheal Intubation

Flexible Tip Bougie Catheter Intubation

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

We, therefore conducted a randomized cross over study to evaluate the usefulness of this new device use by experienced anesthesiologists in several airway manikin scenarios. We hypothesized that in the hands of experienced anesthesiologists the new Flexible Tip Bougie catheter would perform comparably to the standard bougie catheter) in the normal airway scenario. In the difficult airway (both tongue edema, manual in-line stabilization, or cervical collar stabilization), we hypothesized that the new Flexible Tip Bougie catheter would prove superior to the standard Bougie stylet.

NCT ID: NCT03729037 Completed - Clinical trials for Cardiopulmonary Arrest With Successful Resuscitation

Cardiopulmonary Resuscitation Self-training

Start date: August 10, 2016
Phase: N/A
Study type: Interventional

Participants were 45 first-year medical students randomly assigned to cardiopulmonary resuscitation (CPR) self-training using either a video-based presentation or a serious game developed in a 3D learning environment for up to 20 min. Each participant was evaluated on a written, multiple-choice test (theoretical test) and then on a scenario of cardiac arrest (practical test) before and after exposure to the self-learning methods.