FIDNLIntestinal Lipogenesis and Exogenous Lipid Absorption in Healthy and Obese Subjects Before and After Gastroplasty: Impact of Glucose and Fructose
Data Collection
+ other Data
+ other Data
Collected at a single point in time - Cross-sectionalBody Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Case-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
Study start date: February 1, 2013
Actual date on which the first participant was enrolled.This study aims to understand how the intestine processes fats in healthy individuals and obese subjects, including those who have undergone gastroplasty, a type of weight-loss surgery. The study is particularly interested in how the intestine produces new fats from sugars like glucose and fructose. This research could help improve our understanding of how obesity and weight-loss surgery affect the body's fat processing, potentially leading to better care for these conditions. Participants will consume test meals containing different combinations of cream, whey protein, fructose, and glucose. Some meals also include special forms of fructose or palmitic acid that can be traced in the body. After the meal, the study will measure how much new fat the intestine has produced and how quickly the body absorbs fats from the meal. This is done by looking for specific substances in the blood. The study has two parts, each focusing on different aspects of fat processing.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.24 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 25 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Centre Hospitalier Universitaire Vaudois
Lausanne, SwitzerlandOpen Centre Hospitalier Universitaire Vaudois in Google Maps