Monitoring of Hepatic Fat Metabolism Using Magnetic Resonance Methods

NCT03680248 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2020-06-16

No results posted yet for this study

Summary

The first primary research objective of the study is to determine whether high-fat load (150 g of fat) induces increase in hepatic fat content (HFC) three and six hours after meal in insulin-sensitive subjects with normal HFC (\<5% of fat) and in non-diabetic subjects with an increased HFC (\>5% of fat). Furthermore, the other objective of the study is to determine whether the response of HFC to a high-fat load is affected by coadministration of glucose or fructose.

Conditions

  • Hepatic Fat Content

Interventions

DIETARY_SUPPLEMENT

Fat

Subjects will consume dairy cream (150 g of fat) at time 0 hours.

DIETARY_SUPPLEMENT

Fasting

Subjects will fast throughout the experiment.

DIETARY_SUPPLEMENT

Fat+Glucose

Subjects will consume dairy cream (150 g of fat) at time 0 hours. At the same time and 2 and 4 hours later they will drink herbal tea containing 50 g of glucose.

DIETARY_SUPPLEMENT

Glucose

Subjects will drink herbal tea containing 50 g of glucose at times 0, 2 and 4 hours.

DIETARY_SUPPLEMENT

Fat+Fructose

Subjects will consume dairy cream (150 g of fat) at time 0 hours. At the same time and 2 and 4 hours later they will drink herbal tea containing 50 g of fructose.

DIETARY_SUPPLEMENT

Fructose

Subjects will drink herbal tea containing 50 g of fructose at times 0, 2 and 4 hours.

Sponsors & Collaborators

  • Institute for Clinical and Experimental Medicine

    lead OTHER_GOV

Principal Investigators

  • Milan Hajek, DSc · Institute for Clinical and Experimental Medicine

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-04-26
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • Czechia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03680248 on ClinicalTrials.gov