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Post Cardiac Arrest Syndrome clinical trials

View clinical trials related to Post Cardiac Arrest Syndrome.

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NCT ID: NCT05586282 Not yet recruiting - Septic Shock Clinical Trials

Role of Candidate Proteins in Capillary Leakage During Acute Circulatory Failure

Start date: November 2022
Phase:
Study type: Observational

- Testing the association between circulating candidate proteins and the level of vascular leakage for three distinct forms of circulatory failure: cardiogenic shock, septic shock, and post-resuscitation syndrome. - Describing immuno-inflammatory profiles associated with massive vascular leakage during those three forms of circulatory failure in humans

NCT ID: NCT04859270 Not yet recruiting - Clinical trials for Post-Cardiac Arrest Syndrome

The Holistic Health Care of Post-Cardiac Arrest Survivors: From Patient's Health to Family Resilience

Start date: May 1, 2021
Phase:
Study type: Observational

Post-cardiac arrest mortality remains high and proper care after cardiopulmonary resuscitation is an important clinical challenge. This prospective observational cohort aims to (1) identify the factors that affect short-term and long-term survival in post-cardiac arrest survivors and (2) investigate the patients and their families' health-related quality of life and psychological well-being.

NCT ID: NCT04339257 Not yet recruiting - Clinical trials for Out-Of-Hospital Cardiac Arrest

Pre-hospital Post ROSC Care: Are we Achieving Our Targets?

POP-ROC
Start date: May 2020
Phase:
Study type: Observational [Patient Registry]

Rational: Out of hospital cardiac arrest is a devastating event with a high mortality. Survival rates have increased over the last years, with the availability of AED's and public BLS. Previous studies have shown that deranged physiology after return of spontaneous circulation (ROSC) is associated with a worse neurological outcome. Good quality post-arrest care is therefore of utmost importance. Objective: To determine how often prehospital crews (with their given skills set) encounter problems meeting optimal post-ROSC targets in patients suffering from OHCA, and to investigate if this can be predicted based on patient-, provider- or treatment factors. Study design: Prospective cohort study of all patients attended by the EMS services with an OHCA who regain ROSC and are transported to a single university hospital, in order to identify those patients with a ROSC after a non-traumatic OHCA who had deranged physiology and/or complications from OHCA EMS personnel was unable to prevent/deal with in the prehospital environment. Study population: Patients, >18 years, transported by the EMS services to the ED of the University Hospital Groningen (UMCG) with a ROSC after OHCA in a 1 year period Main study parameters/endpoints: Primary endpoint of our study is the percentage of OHCA patients with a prehospital ROSC who arrive in hospital with either a deranged physiology or with complications from OHCA EMS personnel was unable to deal with.