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NCT07378072Recruiting

Efficacy of 12-week Daytime Restricted Eating on Hepatic Steatosis of Obesity

Efficacy of 12-week Daytime Restricted Eating on Hepatic Steatosis of Obesity: Randomized, Open-label, Parallel Group, Controlled Superiority Trial _ CHRONOSTEATOSIS

Source: ClinicalTrials.gov · Last updated 29 Jun 2026

Brief summary (registry, in English)

The objective of this study is to demonstrate that an \< or equal to 8-hour time-restricted eating (i.e., fasting for at least 16 hours every day), not focusing on reducing caloric intake, reduces intra-hepatic fat in patients with obesity and Metabolic dysfunction-Associated Steatotic liver Disease (MASLD).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
72 (estimated)
First submitted
11 Dec 2025
Start date
17 Jun 2026
Primary completion date
Jun 2029
Lead sponsor
Nantes University Hospital
NCT number
NCT07378072

What you commit to

  • Study type: Interventional
  • Planned participants: 72
  • From 17 Jun 2026 to the primary completion date, Jun 2029
  • 9 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.

Prior treatment

  • Medications affecting weight or energy balance

Other illness

  • Chronic liver disease other than MASLD
  • Severe hepatic disease (cirrhosis, hepatocellular carcinoma)
  • Severe cardiac disease (Chronic heart failure classified as being in New York Heart Association (NYHA) Class III or IV)
  • Severe Kidney disease with CKD-EPI\<30 mL/min/1,73m2
  • MRI not possible due to the following (an MRI safety screening form will have to be filled for inclusion): presence of a pacemaker or cardiac defibrillator or cardiovascular catheter or neurostimulator or an implantable electronic pump for automated drug injection or an electronically-controlled implantable chamber. Ocular metallic foreign bodies
  • History of severe eating disorders: Binge Eating Disorder, Bulimia Nervosa; Night eating syndrome

Lab values

  • Patient with diabetes if HbA1c not at target (\<7%) and/or using a non-authorized medication)

Other

  • Alcohol intake \> 20 g/day
  • Night-shift workers or rotating shift workers
  • Smoking
  • Initiation of hormonal treatment during the study period
  • Magnetic Resonance Imaging (MRI) not possible due to patient's anthropometric characteristics. Any of the following:
    • abdominal and/or thoracic circumference with arms greater than 200 cm
    • Sagittal diameter (or abdominal height, i.e. the distance between the dorsum and the apex of the abdomen, which was measured in the supine position at the midpoint between the iliac crest and the last rib) over 70 cm
    • body weight over 160 kg
  • Minors
  • Adults under guardianship, trusteeship or under safeguard of justice
  • Other clinical trial participation that could interfere with the study
  • Pregnant women or women trying to be pregnant
  • Nursing mothers
  • Any treatment triggering hepatic steatosis

Who the study is looking for

  • Body mass index (BMI) between 30.0 and 49.9 kg/m2
  • Age between 18 and 65 years (limits included)
  • Sedentary (light-intensity physical activity less than 1 hour per week) or moderately active (moderate exercise 1 to 2 hours per week). Self-declared criteria.
  • Weight stable for at least 3 months prior to the beginning of the study (gain or loss \<4 kg). Self-declared criteria.
  • Able to give written informed consent
  • Self-reported eating interval \> 12 hours per day
  • Subject who owns a smartphone with access to the internet, and agrees to use it in the study
  • Affiliation with French social security system or beneficiary from such system
  • Fibroscan® Controlled Attenuation Parameter (CAP) \> 300 dB/ms
  • Hepatitis B and C serologies negative (or showing past-infection or protective immunization)

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

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

SiteCityCountrySite status
CHU Angers
Coordinator of this site? Confirm its status
AngersFranceNot yet recruiting
CHU Bordeaux
Coordinator of this site? Confirm its status
BordeauxFranceNot yet recruiting
Chu Dijon Bourgogne
Coordinator of this site? Confirm its status
DijonFranceNot yet recruiting
Chu Lyon
Coordinator of this site? Confirm its status
LyonFranceNot yet recruiting
CHU Marseille
Coordinator of this site? Confirm its status
MarseilleFranceNot yet recruiting
CHU Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceNot yet recruiting
CHU Nantes
Coordinator of this site? Confirm its status
NantesFranceRecruiting
Hôpital Européen Georges Pompidou
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
CHU Rennes
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting

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