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Heart Arrest clinical trials

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NCT ID: NCT02411422 Completed - Heart Arrest Clinical Trials

Comparison of Efficiency Between I-gel Blind Intubation and I-gel Bronchoscopic Intubation During Resuscitation

i-gel_br
Start date: April 2015
Phase: N/A
Study type: Interventional

The investigators will compare conventional intubation using Macintosh laryngoscope, blind endotracheal intubation using i-gel for conduit and bronchoscopic intubation using Ambu-aScope and i-gel. All situation assumed as cardiac arrest. i.e, someone give chest compressions continuously without interruption. Moreover the investigators will compare the type of endotracheal tube. Reinforced tube has more soft tube tip, so the investigators think it is more acceptable for intubation using i-gel as conduit.

NCT ID: NCT02408939 Completed - Cardiac Arrest Clinical Trials

Steroids and Post-resuscitation Infectious (Septic) Complications

Start date: March 2015
Phase:
Study type: Observational

Postresuscitation disease is characterized by post-insult systemic inflammation, adrenal insufficiency, and circulatory failure. Such severe pathology may be associated with increased susceptibility to infectious complications and increased risk of death due to postresuscitation septic shock. The latter may be attenuated by stress-dose steroids. In this re-analysis of synthesized randomized clinical trial (RCT) data, the investigators will use individual patient data from two prior RCTs of in-hospital cardiac arrest (NCT00411879 & NCT00729794), in order to determine the effect of stress-dose steroids on the severity of postresuscitation infectious complications, and more specifically, on the risk of septic shock-associated death.

NCT ID: NCT02401633 Completed - Cardiac Arrest Clinical Trials

Compression Only-CPR Versus Standard-CPR

TANGO2
Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Out-of-hospital cardiac arrest (OHCA) is one of the leading causes of mortality in the industrialized world. Bystander CPR before arrival of the Emergency Medical Service (EMS) is a positive predictor of survival. During the last decade, the best form of bystander CPR has been debated. Chest Compression Only CPR (CO-CPR) has been advocated as a preferable method in situations where the bystander has no previous knowledge in CPR, both because its believed to be equally efficient but also a simplified form of CPR that could lead to a higher incidence of bystander-CPR. The purpose of this study is to perform av run-in period with focus on safety and feasibility prior to the launch of a larger randomized trial which has a primary end-point of survival. This study will compare OHCA with standard CPR (S-CPR; chest compressions and rescue breaths in a 30:2 fashion) compared to CO-CPR.

NCT ID: NCT02399930 Completed - Heart Arrest Clinical Trials

Automated Respiration Rate to Improve Accuracy of the Electronic Cardiac Arrest Risk Triage Score (eCART) Algorithm

Start date: April 2015
Phase: N/A
Study type: Observational

Currently, breathing rate and heart rate are checked by nursing staff manually every few hours and entered into a patient's medical record. The investigators are doing this study to see if a device that will automatically record breathing rate and heart rate every 15 minutes is as accurate as the manual measurement. The investigators will also see if these measurements, taken every 15 minutes, will help us predict adverse events more quickly and accurately than the measurements taken every few hours.

NCT ID: NCT02394977 Completed - Clinical trials for Cardiopulmonary Arrest

Effect of the Cardio First Angle Device on CPR Outcomes

CFA
Start date: January 2014
Phase: N/A
Study type: Interventional

The investigators conducted a randomized, controlled, single-blinded study of patients undergoing CPR for cardiac arrest in the mixed medical-surgical ICUs of four academic teaching hospitals in Tehran, Iran from June 1 to October 31, 2014. Patients were randomized to receive CPR with either standard manual compression, or compression with real-time audiovisual feedback using the Cardio First Angelâ„¢ device.

NCT ID: NCT02391857 Completed - Clinical trials for Out-of-Hospital Cardiac Arrest

Early Gastric Decompression During Advanced Cardiopulmonary Resuscitation (EGD_ACLS)

EGD_ACLS
Start date: March 1, 2015
Phase: N/A
Study type: Interventional

This study aimed to identify the effect of early gastric decompression on the improvement of circulation in arrest patients during cardiopulmonary resuscitation at the clinical setting of emergency department.

NCT ID: NCT02390999 Completed - Cardiac Arrest Clinical Trials

Neurological Prognostication of Patients in Therapeutic Hypothermia After Cardiac Arrest

Start date: March 2013
Phase: N/A
Study type: Interventional

3500 people suffer from out of hospital cardiac arrest each year in Denmark. Therapeutic hypothermia to 33 degrees celsius is now standard treatment of comatose cardiac arrest patients. The investigators are challenged in our attempt to predict outcome of these patients by both low body temperature in itself and the sedative and relaxing drugs used to keep the patient in a coma. This study is a substudy in a large international multicenter randomized trial that investigates the possible benefit of 48 hours of therapeutic hypothermia versus todays standard of 24 hours. In this substudy the investigators will approach early prediction of neurological outcome using a combination of new examinations backed up by well established ones to engage this challenge from different angles and find a battery of combined examinations, that together will enable us to accurately predict outcome at an earlier stage. Our examinations have been chosen from the three fields of neurophysiology, biochemistry and neurology and consist of electroencephalography (EEG), somatosensory evoked potentials (SEP), biomarkers and clinical examinations such as brain stem reflexes chosen for their prognostic reliability.

NCT ID: NCT02387775 Completed - Cardiac Arrest Clinical Trials

Temperature Control With an Esophageal Cooling Device in Post Cardiac Arrest Patients

E-Chill
Start date: December 2015
Phase: N/A
Study type: Interventional

This is a prospective, interventional study aiming to assess the effectiveness of the Esophageal Cooling Device (ECD) as a temperature control modality in post cardiac arrest patients. In addition, observed adverse events during ECD use, ease-of-use, nurse satisfaction and patient outcomes will be examined.

NCT ID: NCT02381977 Completed - Stroke Clinical Trials

Prevalence of Acute Critical Neurological Disease in Children: a Global Epidemiological Assessment

PANGEA
Start date: November 2011
Phase: N/A
Study type: Observational

PANGEA is an international prospective point prevalence study to describe the epidemiology, interventions, and outcomes in children with acute critical brain disease.

NCT ID: NCT02368392 Completed - Clinical trials for In-hospital Cardiac Arrest

National Cardiac Arrest Survey

NCAS
Start date: July 2014
Phase: N/A
Study type: Observational

The aim of this study is to describe incidence of "in-hospital" deaths and outcomes after attempted cardiac arrest resuscitation, availability of resuscitation equipment and medical staff training in state Hospitals of Sri Lanka.