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Heart Arrest clinical trials

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NCT ID: NCT05730114 Recruiting - Clinical trials for Myocardial Infarction

Monitoring Antiplatelet Drugs in Cardiac Arrest Patients

PLT-ECMO
Start date: October 1, 2022
Phase:
Study type: Observational

Dual Antiplatelet Therapy (DAPT) with acetylsalicylic acid (ASA) and oral P2Y12 inhibitor (Clopidogrel, Ticagrelor or Prasugrel) is recommended in STEMI or NSTEMI patients undergoing primary Percutaneous Coronary Intervention (PCI). There is evidence for an increased risk of stent thrombosis after PCI despite administration of DAPT in patients resuscitated from a cardiac arrest with STEMI/NSTEMI who undergo primary PCI, in particular for those treated with hypothermia. Point of Care Aggregometry represents an emerging tool to measure platelet reactivity in patient treated with antiplatelets drugs. Among patients with Acute Coronary Syndrome (ACS), those requiring Veno-Arterial Extracorporeal Membrane Oxygenation (VA-ECMO) for refractory Cardiogenic Shock or Cardiac Arrest represent a growing population burdened by more profound metabolic, pharmacokinetic, hemostatic and physiological alterations due to increased clinical severity and ECMO itself. In addition, profound platelet inhibition can result in a higher risk of bleeding complication, since these patients have to be simultaneously anticoagulated with unfractioned heparin (UFH) and ECMO itself can cause coagulopathy. We aimed to perform an observational prospective cohort study to investigate platelet reactivity in a population of ACS patients with different clinical severity.

NCT ID: NCT05724914 Completed - Cardiac Arrest Clinical Trials

Call to Door Timing in Out-of-hospital Cardiac Arrest

Start date: February 14, 2023
Phase:
Study type: Observational

The investigators aimed to investigate the effect of delayed hospitalization on the basis of the call time on the clinical outcomes of patients with OHCA patients using a nationwide OHCA registry.

NCT ID: NCT05716789 Completed - Cardiac Arrest Clinical Trials

Cardiopulmonary Resuscitation in Cases of Sudden Cardiac Arrest

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Determination the success rate of CPR on adults in Emergency room and predicting the factors that makes CPR is successful.

NCT ID: NCT05712915 Completed - Clinical trials for Cardiopulmonary Arrest

Extension of Rapid Response Team Operation Time and Cardiopulmonary Resuscitation Incidence

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

Although early rapid response team was reported as a full-time operating system, similar efficacy of part-time rapid response team has been recently reported. We sought to investigate the association between the duration of rapid response team operation time and the incidence of general ward cardiopulmonary resuscitation.

NCT ID: NCT05709665 Recruiting - Resuscitation Clinical Trials

Incidence of the Out- and in Hospital Cardiac Arrest at a Tertiary Hospital in Germany

ProseCPR
Start date: January 11, 2023
Phase:
Study type: Observational

Incidence of the background information, incidence and special characteristics of out- and in-hospital cardiac arrest at a tertiary hospital in Germany.

NCT ID: NCT05709613 Completed - Cardiac Arrest Clinical Trials

Use of a Feedback Device to Limit Too Shallow Compressions Associated With the Use of an I-gel® Device

Start date: January 30, 2023
Phase: N/A
Study type: Interventional

Airway management in out-of-hospital cardiac arrest is still debated. Several options exist: bag-valve-mask ventilation, supraglottic devices and endotracheal intubation. Intermediate and advanced airway management strategies could be useful devices to increase chest compression fraction. A previous study shows that early insertion of an i-gel device significantly increases chest compression fraction and enhances respiratory parameters. However, the compressions were found to be shallower in the experimental group using the i-gel device. Although, the shallower compressions found in the supraglottic airway device group did not appear to be linked to their provision in an over-the-head position, it is reasonable to assume that the addition of a feedback device to the use of an i-gel® device could fix this issue. The feedback devices seem to be able to provide a benefit, and allow deeper compressions / more often in the depth target. There is a mismatch between perceived and actual cardiopulmonary resuscitation performance supporting the need for such a feedback device's study.

NCT ID: NCT05706194 Recruiting - Cardiac Arrest Clinical Trials

Early Neuroprognostication After OHCA

Start date: October 1, 2023
Phase:
Study type: Observational

This is a prospective observational substudy of the STEPCARE trial ClinicalTrials.gov Identifier: NCT05564754) with the aim to examine whether prognostication of neurological outcome after cardiac arrest can be performed earlier than the 72 h time-point recommended by guidelines today.

NCT ID: NCT05679739 Recruiting - Clinical trials for Out-Of-Hospital Cardiac Arrest (OHCA)

NEUROprotection Via optimizINg Cerebral Blood Flow afTer cArdiaC arresT (NEURO-INTACT) Study

Start date: August 29, 2023
Phase: N/A
Study type: Interventional

This single-center proof of concept study aims to assess the efficacy of a blood pressure strategy targeting person- and time-specific cerebral blood flow compared with standard-of-care using neuron-specific enolase as a quantitative biomarker of brain injury. Our central hypothesis is that an individualized blood pressure strategy targeting cerebral perfusion, compared with standard-of-care, will reduce the extent of brain injury as indicated by changes in levels of neuron-specific enolase from baseline at 72 hours. To test this hypothesis, the investigators will randomly assign 90 patients to an individualized blood pressure management strategy targeting cerebral blood flow, where optimal blood pressure will be serially calculated by the ICM+ brain monitoring software (Cambridge, UK) using inputs from transcranial Doppler ultrasound and near-infrared spectroscopy (intervention), versus achieving a standard level of systemic blood pressure (standard-of-care). This is done in a 2:1 allocation (60 to intervention, 30 to standard-of-care), in the first 72 hours after return of spontaneous circulation (ROSC).

NCT ID: NCT05646875 Recruiting - Brain Injuries Clinical Trials

A Comprehensive Evaluation of Hyperbaric Oxygen Therapy in Resuscitation Medicine - A Pilot Study (HOT-RESUS 1 Trial)

HOT-RESUS 1
Start date: February 1, 2023
Phase: N/A
Study type: Interventional

In this prospective pilot study, the effects of hyperbaric oxygen therapy (HBOT) in post-cardiac arrest syndrome will be evaluated. However, the primary outcome of this pilot study will be the feasibility of this approach. If feasibility is determined, a larger study with adequate powering is to follow.

NCT ID: NCT05639868 Completed - Cardiac Arrest Clinical Trials

Effectiveness of Video-assisted Cardiopulmonary Resuscitation

Start date: December 1, 2022
Phase: N/A
Study type: Interventional

Sudden cardiac arrest is a major public health problem worldwide and it is one of the leading causes of death in industrialized countries. Emergency Medical Services (EMS) dispatchers play an important role to recognize cardiac arrest and give help to the lay first responder via telephone CPR (T-CPR) which improves survival rates. The current technology allows the live video connection between the scene and the dispatcher which provides the opportunity for video-assisted CPR (V-CPR) via the bystander smartphone. Effectiveness of V-CPR has only been investigated to a limited extent. Comparing effectiveness of V-CPR (effectiveness of chest compression, time parameters eg. time to first chest compression) to T-CPR and non-instructed CPR can be useful to implement V-CPR technology.