healthy volunteers no medical condition
Conditions
Sponsors
KULeuven
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy volunteers (18-45 years) who have no bowel symptoms and who are in good general health are eligible for the study Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 14 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: -they have relevant underlying disease (cardia, pulmonary, metabolic, kidney or liver diseases...) -They have a history of esophageal or gastric surgery, or recurrent or intermittent upper gastrointestinal symptoms (upper abdominal pain, neusea, vomiting, bothersome fullness or early satiation, heartburn, regurgitation...) -They have a history of allergy to several types of drugs or food -They have been treated for depression -There is a possibly of becoming pregnant during the study period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: We set out to investigate the effect of liraglutide on the relation between gastric accommodation and satiation by measuring the IGP in fasted condition and after the intragastric nutrient drink infusion ;Secondary Objective: not applicable;Primary end point(s): liquid nutrient tolerance to reach maximum satiation return of hunger ;Timepoint(s) of evaluation of this end point: none | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): none;Timepoint(s) of evaluation of this end point: none | — |
Countries
Belgium
Contacts
Public ContactAlessandra Rotondo
KULeuven
Outcome results
None listed