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Evaluation of the Severity of Hepatic Fibrosis by Magnetic Resonance Elastography in the Diagnosis of Endogenous Hypercorticism — HEPACORT  

Metabolic Syndrome Clinical Trial

Official title:
Evaluation of the Severity of Hepatic Fibrosis by Magnetic Resonance Elastography in the Diagnosis of Endogenous Hypercorticism

Clinical Trial Summary

The main hypothesis of the HEPACORT study is that upon diagnosis of endogenous Cushing's syndrome, significant liver fibrosis may be present, particularly in the most severe forms of Cushing's syndrome. the HEPACORT study is the first exploratory study to assess the severity of liver fibrosis in patients with Cushing's syndrome or suspected of presenting by Magnetic Resonance Elastography (MRE).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05911620
Study type Interventional
Source Central Hospital, Nancy, France
Contact Nicolas SCHEYER, MD
Phone +33383154302
Email n.scheyer@chru-nancy.fr
Status Recruiting
Phase N/A
Start date October 24, 2023
Completion date August 31, 2026
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