Gastric Layering and Monitoring II (GLAM-II)

Wageningen University

Status

Completed

Conditions

Infant Formula

Treatments

Other: Infant Formula

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT05224947

NL77717.091.21

Details and patient eligibility

About

Rationale: Results from a previous study suggest that gastric layer formation, which is caused by emulsion instability as a result of gastric acidification/digestion, is different between breastmilk and infant formula. The current study focusses on further understanding of these differences by investigating the effect of formula composition.

Objective: To investigate the effect of infant formula composition on intragastric behavior, gastric emptying and postprandial plasma parameters.

Study design: Double-blind cross-over study with two treatments.

Study population: 20 healthy normal-weight males, aged 18-45 y.

Intervention: After an overnight fast, participants will drink sufficient volume of one of the two IFs which differ in composition. Gastric content will be monitored using Magnetic Resonance Imaging (MRI). MRI scans will be done and blood samples will be taken for subsequent analyses at baseline and post prandially .

Main study parameters/endpoints: The primary outcome is gastric behavior. Secondary outcomes are total gastric content volume over time and blood parameters.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The risks associated with participation are low, as both phlebotomy and MRI are eminently safe medical techniques. In addition, the test formula are safe. Each participant will participate in 2 sessions, which require an overnight fast, 9 blood withdrawals (in total 120 mL per visit) and multiple MRI scans over a period of approximately 2 hours. These measurements are non-invasive and carry minimal risk. The burden of the sessions is most likely related to mild discomfort as they have to lie still in the MRI for two hours. This will be minimized by the soft mattress on the bed of the MRI, leg rest and a pillow underneath the head.

Enrollment

20 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male
Apparently healthy (self-reported)
Willing to be informed about incidental findings of pathology
Willing to comply with the study procedures

Exclusion criteria

Allergy or intolerance for cow milk, lactose, soy and/or fish (self-reported)
Gastric disorders or regular gastric complaints, for example heart burn
- Use of medication which alters the normal functioning of the stomach, such as: Medical drug use that influences the GI tract's normal function, e.g. motility, pH etc.: among others use of protein pump inhibitors, antacids, anti-depressants etc. (judged by study doctor)
- Medical drug use that influences the GI tract's microbiota: antibiotic use within one month prior to the pre-study screening day (judged by study doctor)
Smoking (>2 cigarettes a week)
Drinking more than 14 glasses of alcohol a week
Having given a blood donation in the past two months
Hb value below 8.4 mmol/L (as measured with finger-prick method at screening)
Having a contra-indication to MRI scanning, including, but not limited to:
- Pacemakers and defibrillators
- Intraorbital or intraocular metallic fragments
- Ferromagnetic implants
- Claustrophobia
Participating in other research during the study period
Being an employee or student of the division of human nutrition and health
Not having a general practitioner