Phase
Condition
Primary Biliary Cholangitis
Liver Disease
Treatment
adapted physical activity + Dietetic advice
Clinical Study ID
Ages 18-90 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patient aged 18 and over
Affiliated with social security
Signature of informed consent
Diagnosis of NAFLD characterized by the presence of ultrasound steatosis, with adiagnosis made by a physician after a clinical and paraclinical examination as isusually done in routine care and having eliminated another cause of chronic liverdisease.
Effective contraception system for women of childbearing age, a urine pregnancy testwill be offered to these women as part of the assessment of the screening visit.
Exclusion
Exclusion Criteria:
Patient under legal protection
Refusal to participate in the study
Alcohol consumption ≥ 30 g/d for men or ≥ 20 g/d for women
Presence of chronic liver disease from causes other than NAFLDs
Inability to obtain 10 valid measurements when performing a FibroScan liverelasticity measurement or continuous CAP® steatosis assessment during initialevaluation.
FibroScan ≥ 20 kPa at initial assessment
Presence or history of advanced chronic liver disease (cirrhosis) decompensated (Child A6, B or C).
Known history of a complication related to portal hypertension (including digestivehaemorrhage related to portal hypertension, ascites or pleural effusion of cirrhoticcirrhosis, port-pulmonary hypertension).
Notion of type 2 diabetes unbalanced with an HbA1c ≥ 9%, less than 3 months (measurement of HbA1c is not required before signing the consent form).
Platelets < 150000/mm3, within the previous 6 months.
Type 1 diabetes
Weight loss ≥ 10% of usual body weight, in the 6 months prior to inclusion
Introduction or dose modification of a GLP1 or orlistat agonist treatment < 1 year
Practice of regular and/or intense physical activity, weekly (more than 3 hours perweek)
Patients with solid organ or bone marrow transplants
Patient participating in another study evaluating a therapy to improve non-alcoholicfatty liver disease (NAFLD)
Contraindication to carrying out APA:
Absolute contraindication criteria:
Any unstable pathology affecting a vital organ in particular cardiovascular or pulmonary. Unstable means any situation in which the absence of urgent therapeutic intervention could lead to the death of the patient.
o Contraindication to physical activity Unstable acute coronary syndrome Decompensated heart failure Severe, uncontrolled ventricular rhythm disturbances Presence of an intracardiac thrombus with high embolic risk Presence of a medium to large pericardial effusion Recent history (<6 months) of thrombophlebitis with or without pulmonary embolism Severe and/or symptomatic left ventricular ejection obstruction Any progressive inflammatory and/or infectious disease Severe pulmonary arterial hypertension
Study Design
Study Description
Connect with a study center
CHU de Nice
Nice, 06000
FranceSite Not Available
Ch de Perpignan
Perpignan, 66046
FranceSite Not Available
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