Clinical trials: Resuscitations
High-fidelity Simulation
High-Fidelity Simulation
This study explores the impact of high-fidelity simulation-based training on critical care nurses' emergency knowledge, skills, and teamwork in emergency and intensive care units.
- Trial name
- NCT06935773
- Testing
- High-Fidelity Simulated Emergency Training, No intervention (observational study)
- Where
- Taiwan
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Pei Yu Huang
Cardiac Arrest, Fibrillation, Ventricular
Early Double Sequential Defibrillation in Out-of-hospital Cardiac Arrest
Some of the patients affected by Out-of-hospital cardiac arrest (OHCA) with ventricular fibrillation (VF)/ventricular tachycardia (VT) do not respond to initial defibrillation.
- Conditions
- Cardiac Arrest, Fibrillation, Ventricular, Sudden Cardiac Death, Sudden Cardiac Arrest
- Trial name
- DOUBLE-D (NCT06447805)
- Testing
- Double Sequential Defibrillation (DSD), Standard defibrillation
- Where
- 3 sites in Sweden
- Volunteers
- 40 people
- Sponsor
- Karolinska Institutet
eFast Diagnosis Performance in Guiding First Aid Resuscitation and Hemostasis
eFast Diagnosis Performance in Guiding First Aid Resuscitation
A lesion work-up associating clinical examination, extended focused ultrasound (eFAST including abdominal ultrasound [right upper, left upper, and suprapubic quadrant], bilateral anterior and lateral pleuropulmonary ultrasound…
- Trial name
- eFAST Decision (NCT03699670)
- Where
- France
- Volunteers
- 510 people
- Sponsor
- University Hospital, Grenoble
Cardiopulmonary Arrest
Usefulness of the Evaluation of the ROSC With Carotid Ultrasound During CPR
The current cardiopulmonary resuscitation(CPR) guidelines recommend that the heart rhythm be checked every two minutes during CPR for cardiac arrest patients.
- Trial name
- NCT04793386
- Testing
- carotid ultrasound
- Where
- South Korea
- Volunteers
- 23 people
- Sponsor
- Samsung Medical Center
Cardiac Arrest
Pragmatic Airway Resuscitation Trial
The primary objective of the trial is to determine if 72-hour survival after out-of-hospital cardiac arrest (OHCA) is improved with initial endotracheal intubation (ETI) over initial laryngeal tube (LT) airway management…
- Trial name
- PART (NCT02419573)
- Testing
- Endotracheal Intubation, Laryngeal Tube (King)
- Where
- 6 sites in United States
- Volunteers
- 3,004 people
- Sponsor
- University of Alabama at Birmingham
Cardiac Arrest, Reanimation
Study of the Occurrence of Cardiocirculatory Arrest as a Function of the Level of Hypoxemia During a Maastricht 3 Procedure
Evaluation of the level of hypoxemia during the occurrence of cardiocirculatory arrest during a Maastricht III organ donation procedure.
- Trial name
- HEPHAISTOS (NCT06780722)
- Testing
- blood sampling
- Where
- 12 sites in France
- Volunteers
- 50 people
- Sponsor
- Nantes University Hospital
Out-Of-Hospital Cardiac Arrest
Selective Cerebral Hypothermia Trial - Under Extracorporeal Cardiopulmonary Resuscitation (SHOT-ECPR)
The study is designed as a pilot, open-label study to investigate the feasibility and safety of selective cerebral hypothermia in OHCA patients receiving ECPR.
- Trial name
- NCT03345706
- Testing
- Selective cerebral hypothermia, Regular hypothermia
- Where
- Taiwan
- Volunteers
- 20 people
- Sponsor
- National Taiwan University Hospital
Blunt Trauma, Penetrating Wound
Field Trial of Hypotensive Versus Standard Resuscitation for Hemorrhagic Shock After Trauma
Primary Aim: To determine the feasibility and safety of hypotensive resuscitation for the early treatment of patients with traumatic shock compared to standard fluid resuscitation.
- Conditions
- Blunt Trauma, Penetrating Wound, Hemorrhagic Shock
- Trial name
- HypoResus (NCT01411852)
- Testing
- 0.9% Sodium Chloride 250 mL bolus, 0.9% Sodium Chloride 2000 mL bolus
- Where
- 6 sites in United States, Canada
- Volunteers
- 192 people
- Sponsor
- University of Washington
Cardiopulmonary Arrest
Comparison of Tracheal Ultrasound With Capnography for Intubation Confirmation During CPR Wearing PPE
It is very important to ensure the tube placement in patients with cardiac arrest and unrecognized misplacement of endo-tracheal tube can lead to morbidity and mortality.
- Trial name
- NCT04690517
- Testing
- tracheal ultrasound
- Where
- South Korea
- Volunteers
- 34 people
- Sponsor
- Samsung Medical Center
Septic Shock
Protocolised Early De-Resuscitation in Septic Shock (REDUCE)
Background: Recent studies have questioned the safety of current fluid resuscitation strategies in patients with septic shock as prospective and observational data suggesting that the resulting fluid overload is associated with…
- Trial name
- REDUCE (NCT04931485)
- Testing
- Fluid management according to the REDUCE Fluid Protocol, Standard of care
- Where
- 4 sites in Switzerland
- Volunteers
- 170 people
- Sponsor
- Insel Gruppe AG, University Hospital Bern
Sudden Unexplained Infant Death, Apnea of Newborn
Advanced Wireless Sensors for Neonatal Care in the Delivery Room
The goals of this observational study is to assess whether a new advanced wireless skin sensor vital sign monitoring system can effectively monitor the vital signs of healthy newborn infants (≥ 35 weeks gestational age).
- Conditions
- Sudden Unexplained Infant Death, Apnea of Newborn, Newborn Morbidity, Newborn Asphyxia
- Trial name
- AWARD (NCT06693817)
- Testing
- Wireless skin sensors vital sign monitoring system, Wired vital sign monitoring system
- Where
- 5 sites in Brazil, Canada and 2 more
- Volunteers
- 600 people, healthy volunteers welcome
- Sponsor
- Guilherme Sant'Anna, MD
Fluid Therapy
Crystalloid FLUID Choices for Resuscitation of Hospital Patients
Salt fluids are used extensively for acutely ill patients who are admitted to hospital. Two salt fluids commonly used are Normal Saline and Ringer's Lactate.
- Trial name
- FLUID (NCT02721485)
- Testing
- Ringer's Lactate, Normal Saline
- Where
- 4 sites in Canada
- Volunteers
- 30,000 people
- Sponsor
- Ottawa Hospital Research Institute
Virtual Reality, Neonatal Resuscitation
Effectiveness of VR and LR Applications in Newborn Resuscitation Education
This research was designed to investigate the effectiveness of virtual reality and low reality simulation applications in neonatal resuscitation skills training.
- Conditions
- Virtual Reality, Neonatal Resuscitation, Simulation
- Trial name
- NCT06776211
- Testing
- Virtual Reality Simulation, Low-Reality Simulation
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Saglik Bilimleri Universitesi
Meconium Aspiration Syndrome, Infant, Newborn, Disease
Time of Positive Pressure Ventilation in Non-vigorous Infants Born Through Meconium-stained Amniotic Fluid
Background: Meconium stained amniotic fluid (MSAF) complicates 3 to 14% of pregnancies, causing meconium aspiration syndrome (MAS) in 5-10% of neonates born.
- Conditions
- Meconium Aspiration Syndrome, Infant, Newborn, Disease, Neonatal Resuscitation
- Trial name
- MASTIME (NCT04076189)
- Testing
- Endotracheal suctioning, No endotracheal suctioning
- Where
- 2 sites in Italy
- Volunteers
- 40 people
- Sponsor
- University Hospital Padova
Damage Control, Trauma Abdomen
BIA Guided-fluid Management in Postinjury Open Abdomen
Fluid overload (FO), resulting from high volume fluid therapy, is frequent and contributes to excessive visceral edema, delayed fascial closure, and adverse outcomes among postinjury open abdomen (OA) patients.
- Conditions
- Damage Control, Trauma Abdomen, Acute Compartment Syndrome
- Trial name
- BGFM (NCT03466684)
- Testing
- BIA-guided fluid resuscitation protocol, Traditional fluid resuscitation protocol
- Volunteers
- 140 people
- Sponsor
- Nanjing PLA General Hospital
Respiratory Depression Neonatal
Bedside Improvement of Resuscitation Through mHealth Feedback (BIRTH Study)
Purpose: To evaluate the effectiveness of newborn resuscitation feedback supported by a mobile health application called LIVEBORN; secondarily, to evaluate the relative effectiveness of real-time guidance vs debriefing.
- Trial name
- NCT05963516
- Testing
- LIVEBORN: A Mobile Health Application (app) for Newborn Resuscitation, NeoBeat: Heart Rate Meter for Newborn Resuscitation
- Where
- 4 sites in Democratic Republic of the Congo
- Volunteers
- 14,679 people, healthy volunteers welcome
- Sponsor
- University of North Carolina, Chapel Hill
Chronic Stress, Cardiac Arrest (CA)
The Role of Stress in Cardiac Arrest (Cortizol CPR)
The aim of this study is to assess long-term stress in patients after an out-of-hospital cardiac arrest. To do this, we will measure levels of the stress hormone cortisol in hair samples.
- Conditions
- Chronic Stress, Cardiac Arrest (CA), Post-Resuscitation Syndrome, Heart Attack
- Trial name
- Cortizol (NCT07285915)
- Testing
- Sample of hair
- Where
- Czechia
- Volunteers
- 136 people
- Sponsor
- University Hospital Pilsen
Out-of-hospital Cardiac Arrest
Prehospital Resuscitation Intra Nasal Cooling Effectiveness Survival Study
Promising result of intra-arrest cooling on neurological intact survival in cardiac arrest patients has recently been published in the PRINCE-study in Circulation 2010.
- Trial name
- PRINCESS (NCT01400373)
- Testing
- Prehospital intra-nasal cooling with RhinoChill
- Where
- 2 sites in Belgium, Sweden
- Volunteers
- 700 people
- Sponsor
- Karolinska Institutet
Cardiac Arrest
Non Invasive Neuromonitoring After Cardiac Arrest
Cardiac Arrest is among the leading causes of death, with survival still well under 50% and the majority of the survivors suffering from moderate to severe neurologic deficits. The human, social and economic costs are staggering.
- Trial name
- NINCA (NCT02575196)
- Testing
- Non-invasive cerebral flow monitoring
- Where
- United States
- Volunteers
- 21 people
- Sponsor
- Icahn School of Medicine at Mount Sinai
Cardiac Arrest
Quality of Chest Compressions After a Night Shift
The investigators sought to evaluate the influence of fatigue after a night shift on the quality of Chest Compressions (CC) in CardioPulmonary Resuscitation (CPR), among physicians.
- Trial name
- WeCAN (NCT02123810)
- Testing
- CPR
- Where
- France
- Volunteers
- 46 people, healthy volunteers welcome
- Sponsor
- Bistro Study Group
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