Clinical Trials Logo

Resuscitation clinical trials

View clinical trials related to Resuscitation.

Filter by:

NCT ID: NCT02625883 Completed - Resuscitation Clinical Trials

Out-of-Hospital Resuscitation in Winterthur - an Outcome Study

Start date: December 2015
Phase:
Study type: Observational

The investigators will retrospectively examine all patients with out-of-hospital resuscitation by the emergency medical Team (EMT) from the Kantonsspital Winterthur in the year 2013 with a two year follow-up and a structured interview about Quality of life. Furthermore, the costs generated by the local health system are analysed.

NCT ID: NCT02575573 Completed - Resuscitation Clinical Trials

Resuscitation Decisions in the Emergency Department (ED)

REDEED
Start date: October 2015
Phase: N/A
Study type: Observational

The investigators will retrospectively examine the connection between resuscitation decisions of admitted patients at the ED of the University Hospital of Basel and several demographic and health related measures. Additionally there will be an examination, which patient characterestics may have lead to patients not having been asked about resuscitation decisions.

NCT ID: NCT02277418 Completed - Intubation Clinical Trials

Venner a.p. Advance Video Laryngoscope

VAVL
Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this study was to compare the Venner a.p. advance video laryngoscope to Miller laryngoscope during resuscitation with and without chest compressions.

NCT ID: NCT02277405 Recruiting - Intubation Clinical Trials

Pediatric Intubation During Resuscitation

PIDR
Start date: October 2014
Phase: N/A
Study type: Interventional

The aim of the study was to compare time and success rates of four intubation devices in a cardiopulmonary scenario with and without chest compressions with a standardized pediatric manikin model.

NCT ID: NCT02275520 Completed - Resuscitation Clinical Trials

Intraosseous Access

NIO
Start date: December 2014
Phase: N/A
Study type: Interventional

The investigators will compare the success rates and time to successful IO access during simulated adult resuscitation.

NCT ID: NCT01875900 Completed - Resuscitation Clinical Trials

Instructor-led Simulation Training Versus Self-directed Simulator Training During Simulated Neonatal Resuscitation

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

Simulation-based training has been widely implemented in medical education. According to educational theories, simulation-based medical education (SBME) is associated with significant advantages, which has been investigated and proved by many studies. However, the value of SBME in comparison to other instructional methodologies remains largely unknown. Therefore, the aim of this study is to directly compare two instructional methods for neonatal resuscitation training.

NCT ID: NCT01774214 Completed - Shock Clinical Trials

Pediatric Fast Fluid Trial 2

PFFT2
Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine which of two commonly used methods of manual pediatric fluid resuscitation (The "Push-Pull Technique" vs. the "Disconnect-Reconnect Technique") allows for the most rapid administration of normal saline when this is urgently required.

NCT ID: NCT01197807 Completed - Resuscitation Clinical Trials

Oronasopharyngeal Suction Versus Simple Nose and Mouth Wiping in Term Newborns

TermWIPE
Start date: November 2010
Phase: N/A
Study type: Interventional

Until recently, bulb or catheter oronasopharyngeal suctioning (ONPS) of all the infants, including vigorous infants in the delivery room, has been featured as a standard of newborn care. The 5th edition of the Newborn Resuscitation Program (NRP) has minimized the recommendation for routine suctioning of infants following delivery, provided they are not depressed or in need of immediate resuscitation. However, this new alternative recommendation was based on a small randomized trial and other lower level evidence rather than evidence from larger trials. The NRP Textbook cautions against vigorous suctioning because of the resultant apnea or bradycardia. Furthermore, suctioning may delay other more important steps of resuscitation. Thus, it is necessary to compare the alternative recommended practice, i.e. simple wiping of the mouth, to determine if it has equivalent efficacy and a favorable side effect profile compared to suctioning.

NCT ID: NCT00719498 Completed - Cardiac Arrest Clinical Trials

Effect of Early High-dose Epoetin Alfa During Cardiac Arrest (Pilot Study)

Start date: November 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the possible neuroprotective effect of early high dose erythropoietin alpha after out of hospital cardiac arrest (OHCA).

NCT ID: NCT00631098 Completed - Resuscitation Clinical Trials

Cannulation for Resuscitation

CARE
Start date: March 2004
Phase: Phase 4
Study type: Interventional

International CPR guidelines recommend the cannulation of a peripheral vein (antecubital or external jugular) during resuscitation. One reason for preferring the external jugular vein over more peripheral veins is the faster circulation time of drugs during CPR. The differences in circulation time may be over 90 seconds between peripheral and central (internal jugular) veins. However, cannulation of the external jugular vein may be more difficult and time consuming than cannulating cubital veins. There are no studies on the success rate, cannulation time and reliability of venous access comparing central and peripheral cannulation sites. We hypothesized that cannulation of the external jugular vein (by paramedics and is a demanding procedure in an emergency situation and should not be recommended during resuscitation. The aims of this study are to compare the feasibility of cannulating the external jugular vein compared to the cubital vein in terms of attempts, cannulation time and reliability of venous access.