Non-alcoholic Fatty Liver Disease in Low Birth Weight Individuals

Recruiting N/A Interventional Study
NAFLD
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
35 – 40
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
8 (estimated)
Sponsor
Steno Diabetes Center Copenhagen · Other
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About This Trial
The investigators will conduct a proof-of-principle 4-weeks low-calorie diet (LCD) intervention study in low birth weight (LBW) subjects and normal birth weight (NBW) controls with documented (MR scan) liver fat content equal to or above 5%. The investigators will provide extended in-depth mechanistic insight into the role of impaired subcutaneous adipose tissue (SAT) expandability in ectopic fat …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * subjects with NAFLD (liver fat content ≥5% liver fat content verified on MRS in the screening NAFLD study) Exclusion Criteria: * BMI\<18.5 and BMI\>30 kg/m2 * Family history of diabetes (siblings, parent, and grandparents) * Disease/medication known to affect primary outcome…
Contacts

Charlotte Brøns, PhD

+4526129093

charlotte.broens.01@regionh.dk

CONTACT