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NCT05881005Recruiting

NAC- NAFLD And Cushing

Prévalence de la stéato-fibrose hépatique Dans le Syndrome de Cushing

Source: ClinicalTrials.gov · Last updated 10 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
5 May 2023
Start date
28 Sept 2023
Primary completion date
28 Sept 2027
Lead sponsor
University Hospital, Angers
NCT number
NCT05881005

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 28 Sept 2023 to the primary completion date, 28 Sept 2027
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Other common causes of chronic liver disease (HBV, HCV, haemochromatosis, alcohol)

Other

  • Contraindication to MRI

Who the study is looking for

  • Age \> 18 years
  • Active Cushing's syndrome

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Angers
Coordinator of this site? Confirm its status
AngersFranceRecruiting
University Hospital Bordeaux
Coordinator of this site? Confirm its status
BordeauxFranceRecruiting
University Hospital Brest
Coordinator of this site? Confirm its status
BrestFranceRecruiting
university Hospital Grenoble
Coordinator of this site? Confirm its status
GrenobleFranceRecruiting
University Hospital Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
University Hospital Nantes
Coordinator of this site? Confirm its status
NantesFranceRecruiting
University Hospital, Nancy
Coordinator of this site? Confirm its status
Vandœuvre-lès-NancyFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.