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Clinical Trials in France / NCT05881005
Recruiting Not applicable

NAC- NAFLD And Cushing

NCT05881005 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-09-28
Last updated
2026-07-10

Condition(s) studied

Cushing SyndromeFatty Liver Disease

Investigational drug(s) / intervention(s)

hepatic MRI

hepatic MRI: Quantification of hepatic steatosis with RMI at the diagnosis (T0) and one year after remission (T1). The percentage of patients with complete resolution of hepatic steatosis on MRI will be determined.

Study summary

Cushing's Syndrome is a rare disease resulting from prolonged exposure to high levels of circulating cortisol. Clinical manifestations are variable but many patients present a metabolic syndrome (abdominal obesity, insulin resistance, dyslipidemia, hypertension). With regard to the liver, experimental data have shown that excess cortisol leads in an increase in lipogenesis and a reduction in the oxidation of fatty acids. This, in association with an accumulation of visceral adipose tissue and deregulation of adipokines, may contribute to the development of hepatic steatosis in animals. However, few data is available in humans with only one study of 50 patients with Cushing's syndrome estimating the prevalence of hepatic steatosis at 20%.

NAFLD (Non-Alcoholic Fatty Liver Disease), is defined as the presence of hepatic steatosis in the absence of secondary causes of intrahepatic fat accumulation. It is a heterogeneous disease ranging from simple liver steatosis, whose prognosis is generally considered to be benign, to inflammation (NASH, Non-Alcoholic Steato-Hepatitis) which may progress to fibrosis, cirrhosis and an increased risk of hepatocellular carcinoma. The prognosis for NAFLD is mainly related to the severity of hepatic fibrosis.

In Cushing's syndrome, normalization of cortisol production is the most effective strategy to improve co-morbidities associated with hypercortisolism. However, some of these complications, especially the metabolic co morbidities, could not be completely reversible and no data is available about resolution of hepatic steatosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \> 18 years * Active Cushing's syndrome Exclusion Criteria: * Other common causes of chronic liver disease (HBV, HCV, haemochromatosis, alcohol) * Contraindication to MRI

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
University Hospital, Angers Angers France Recruiting
University Hospital, Bordeaux Bordeaux France Recruiting
University Hospital, Brest Brest France Recruiting
University Hospital, Grenoble Grenoble France Recruiting
University Hospital, Lille Lille France Recruiting
University Hospital, Nantes Nantes France Recruiting
University Hospital, Nancy Vandœuvre-lès-Nancy France Recruiting

More University Hospital, Angers 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 NCT05881005 on ClinicalTrials.gov ↗ ← All trials in France