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Resuscitation clinical trials

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NCT ID: NCT03773861 Completed - Clinical trials for Educational Problems

Group Size in Basic Life Support (BLS) Courses

Start date: December 10, 2018
Phase: N/A
Study type: Interventional

Basic Life Support (BLS) is important for outcome in cardiac arrest.Therefore, it is crucial to improve the quality of education in resuscitation training. Better training will eventually lead to more effective CPR skills in course participants. BLS courses in both international resuscitation associations (European Resuscitation Council and American Heart Association are typically taught in small groups of 6 participants. In reality group sizes of up to 10 participants are used, because these courses are highly demanded and cost intensive. There is no evidence for the effective group size to be clinical and cost effective. Therefore the investigators perform this prospective study to determine the maximum number of participants an instructor can oversee without missing more than 20% of errors made during an instructional BLS session.

NCT ID: NCT03759210 Recruiting - Clinical trials for Out-Of-Hospital Cardiac Arrest

Outcome After Out of Hospital Cardiac Arrest in Bern, Switzerland

Start date: December 15, 2018
Phase:
Study type: Observational

Sudden cardiac arrests is one of the most frequent causes of death. In Switzerland every year 8000-10.000 people suffer from a cardiac arrest. The EuReCa ONE Study showed regional differences in incidence and chances of survival after cardiac arrests in Europe. The current European Resuscitation Council (ERC) resuscitation guidelines 2015 recommend extracorporeal membrane oxygenation (ECMO) as treatment option for therapy refractory out-of-hospital cardiac arrests (OHCA). ECMO used under cardiopulmonary resuscitation (CPR) is called eCPR (extracorporeal CPR). In the year 2018 eCPR is started to be used in Bern, Switzerland. This study investigates retrospectively the survival and neurologic outcome of patients after OHCA in the region of Bern, Switzerland from 2015-2018. The data will be used as baseline for a prospective evaluation of eCPR cases. The prospective Evaluation of e CPR will last from 2018 - 2022.

NCT ID: NCT03632837 Recruiting - Inflammation Clinical Trials

HaemoAdsorption Nach Reanimation An ECMO

HANRAE
Start date: October 2018
Phase: N/A
Study type: Interventional

This study evaluates the use of an additional hemoadsorption device in adult patients undergoing veno-arterial extracorporal membrane oxygenation (ECMO) following cardiac arrest and cardiopulmonary resuscitation in respect to its effects on post resuscitation inflammatory syndrome. At implantation of the ECMO the participants are going to be randomized into a treatment and a control group. The first will be outfitted with a polymer-based adsorption device implemented in the extracorporal circulation established by ECMO for 48h, the control group is going to be treated by ECMO and standard intensive care alone. To detect any significant differences in terms of inflammatory response and patient outcome the investigators will regularly determine the blood levels of certain cytokines in fixed intervalls. In addition, the investigators are going to compare secondary clinical outcome parameters like organ disfunction and 30d mortality.

NCT ID: NCT03345888 Recruiting - Resuscitation Clinical Trials

To Compare Predictive Power of End-tidal Carbon Dioxide Between Different Time Line During Resuscitation

Start date: November 10, 2017
Phase: N/A
Study type: Observational

To analyze a multi-center observational study database. to select adult non-traumatic in-hospital cardiac arrest. Review and recored end-tidal carbon dioxide in per minute. Arrange them in different time line. one is in resuscitation time. The other is the time line which the beginning time is the time of starting appearing stable end-tidal carbon dioxide wave.To compare predictive power of end-tidal carbon dioxide between different time line during resuscitation.

NCT ID: NCT03326635 Completed - Resuscitation Clinical Trials

Prevalence Study : Elderly Patients and Rehabilitation in ICU. Impact of Frailty.

FRAGIREA
Start date: April 8, 2018
Phase:
Study type: Observational

Study design. The study FRAGIREA is a multicentric prevalence study on the frequency of frailty among elderly patients and the quality of management. The voluntary ICUs will have to include all patients ≥ 70 years on a limited period (1 month) or until the number of 15 inclusions is reached. The frailty is going to be evaluated by a frailty score adapted to the ICU, based on informations given by the patient's family. It is a descriptive non-interventional study, aiming at the description of frequency of frailty and management of the patient in order to set-up a prospective future study on the potential role of early rehabilitation of ageing patients in ICUs.

NCT ID: NCT03256578 Completed - Resuscitation Clinical Trials

Monitoring Neonatal Resuscitation Trial

MONITOR
Start date: February 20, 2017
Phase: N/A
Study type: Interventional

This is a randomized trial to determine if a visible respiratory function monitor (RFM) displaying realtime measurements of delivered inflations improves clinical providers ability to perform positive pressure ventilation (PPV) within a pre-defined target tidal volume in preterm infants after birth.

NCT ID: NCT03225885 Completed - Premature Birth Clinical Trials

Counseling for Prematurity Using a Multimedia Education Tool

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

This study evaluates the effectiveness of prenatal counseling when verbal counseling is supplemented with a multi-media mobile application versus a written gestational age handout.

NCT ID: NCT03114787 Terminated - Resuscitation Clinical Trials

Does Respiratory Physiotherapy Allow for Earlier Withdrawal of Mechanical Ventilation in Respiratory Resuscitation Service?

KISEVEN
Start date: August 30, 2016
Phase: N/A
Study type: Interventional

Respiratory physiotherapy is not routinely prescribed in the resuscitation department and few studies deal with this subject, especially in respiratory resuscitation

NCT ID: NCT03021122 Completed - Pediatrics Clinical Trials

Reducing Medication Errors and Time to Drugs Delivery During Pediatric Cardiopulmonary Resuscitation: a Multicenter RCT

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

The investigators recruit nurses working in 5 swiss Pediatric Emergency Departments or divisions to prepare continuous infusions of vasoactive drugs during a simulation-based pediatric CPR cardiac arrest scenario. According to randomization, nurses will have to prepare and deliver vasoactive drugs following their current conventional methods or by the aim of a mobile tablet application called PedAMINES™. PedAMINES™ is designed to support them step-by-step from order to delivery of these drugs. 1. Primary outcome will be to measure in each allocation group the number of medication dosage errors committed during each drug preparation sequence until injection. 2. Secondary outcome will be to measure the time to drug preparation (TDP) and time to drug delivery (TDD).

NCT ID: NCT02700867 Completed - Resuscitation Clinical Trials

Trial Comparing Proximal Tibia and Proximal Humerus Infusion Rates Using the NIO Intraosseous Device

IOACS
Start date: February 2016
Phase: N/A
Study type: Interventional

The investigators sought to compare the intraosseous access success rates of the proximal tibia and the proximal humerus using new Intraosseous access device "NIO" in an adult cadaver model during simulated resuscitation.