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Clinical Trials in France / NCT05586282
Recruiting Observational

Role of Candidate Proteins in Capillary Leakage During Acute Circulatory Failure

NCT05586282 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2023-03-20
Last updated
2024-10-15

Condition(s) studied

Cardiogenic ShockPostresuscitation DiseaseSeptic Shock

Study summary

* 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

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Informed consent from patient or a legal representative/family member/close relative. The patient will be asked to give his/her consent for the continuation of the trial when his/her condition will allow. 2. Affiliation to social security (AME excluded) 3. Patient with one of the circulatory failures described below: * septic shock * cardiogenic shock * post-resuscitation syndrome * Cardiogenic shock: * Need for a catecholamine support to maintain mean arterial pressure\>65 mmHg, AND * Cardiac index \<2 L/min/m2 or left ventricular ejection fraction (LVEF)\<35%, AND * Lactate \>2.0 mmol/l * Post-resuscitation syndrome: * Cardiac arrest (absence of spontaneous respiration, palpable heartbeat, and responsiveness to stimuli\> 1 min) with a compatible electrocardiogram (asystole/pulseless electrical activity/ventricular tachycardia), AND * Need for a catecholamine support to maintain mean arterial pressure\>65 mmHg, AND * Lactate \>2.0 mmol/l * Septic shock: * Suspected or proven bacterial infection * Need for a vasopressor support to maintain mean arterial pressure\>65 mmHg * Lactate \>2.0 mmol/l * Cardiac index\>3L/min/m2 or LVEF\>40% Exclusion Criteria: 1. Onset of shock (catecholamine infusion) \>12 hours prior to inclusion 2. Age \<18 year old 3. Pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hôpital Européen Georges Pompidou Paris France Recruiting

More Assistance Publique - Hôpitaux de Paris trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05586282 on ClinicalTrials.gov ↗ ← All trials in France