Actively Recruiting
Evaluation of the HPA Axis in Patients With Vasoplegic Syndrome After Cardiac Surgery
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-01-30
200
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Vasoplegic syndrome after cardiac surgery is common and is associated with increased morbidity and mortality. It is characterized by early and prolonged arterial hypotension, with preserved cardiac output and low systemic vascular resistance. Vasoplegic syndrome therefore shares pathophysiological features with septic shock. There are no data in the literature on the function of the hypothalamic-pituitary-adrenal (HPA) axis during vasoplegic syndrome after cardiac surgery. In situations of acute stress and systemic inflammation, relative adrenal insufficiency has been reported in the most severe patients, particularly those in septic shock. The term ""CIRCI"" (Critical Illness-Related Corticosteroid Insufficiency) is currently defined as an increase in total plasma cortisol of less than 9 µg/dl after stimulation with 250 µg tetracosactide (synthetic ACTH), or a basal total plasma cortisol level of less than 10 µg/dl. However, recent studies have called into question the usefulness of the cosyntropin stimulation test for exploring the HPA axis in intensive care patients. Tandem mass spectrometry (LC-MS/MS) assays can be used to measure steroid metabolites (steroidome), enabling more precise exploration of the corticotropic axis. The aim of this study is to evaluate, on an exploratory basis, the impact of the presence of a post-cardiac surgery vasoplegic syndrome on adrenal function by steroidome mapping (LC-MS/MS).
CONDITIONS
Official Title
Evaluation of the HPA Axis in Patients With Vasoplegic Syndrome After Cardiac Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Scheduled cardiac surgery with extracorporeal circulation
- Patient or legal representative informed and has expressed non-opposition to study participation
You will not qualify if you...
- Treatment with glucocorticoids, azoles, phenytoin, rifampin, glitazones, imipraminics, barbiturates, or phenothiazines within the last 3 months
- Adrenal or intracranial pathology affecting the hypothalamic-pituitary axis
- Previous cardiac transplant
- Post-operative mechanical extracorporeal assistance
- Patient deprived of liberty by judicial or administrative decision
AI-Screening
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Trial Site Locations
Total: 1 location
1
Pitié-Salpêtrière
Paris, Île-de-France Region, France, 75013
Actively Recruiting
Research Team
A
Adrien Bouglé, MD, PhD
CONTACT
J
Jérémie Guillemin, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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