Actively Recruiting

Age: 18Years +
All Genders
NCT06371976

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Pitié-Salpêtrière

Paris, Île-de-France Region, France, 75013

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Evaluation of the HPA Axis in Patients With Vasoplegic Syndrome After Cardiac Surgery | DecenTrialz