Gut Hormones and Nutritional Status After a Standardized Meal. (NCT07625319) | Clinical Trial Compass
CompletedNot Applicable
Gut Hormones and Nutritional Status After a Standardized Meal.
Poland80 participantsStarted 2025-04-08
Plain-language summary
This study evaluated differences in serum concentrations of selected gut hormones (GLP-1, GIP, cholecystokinin, and omentin) among individuals with varying nutritional status following a standardized meal.
A total of 80 adults were enrolled and stratified by BMI. Fasting and postprandial hormone levels were assessed at multiple time points.
Additionally, dietary habits, physical activity, body composition, and resting energy expenditure were evaluated to explore their association with hormonal responses.
Who can participate
Age range
40 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* women and men aged 40-60
Exclusion criteria:
* disorders of carbohydrate metabolism,
* endocrine disorders,
* renal and/or hepatic insufficiency,
* gastrointestinal diseases,
* history of gastroenterological or bariatric surgery,
* pharmacological treatment or use of other agents with known or unknown effects on metabolic and hormonal processes,
* other diseases potentially affecting the obtained results,
* pregnancy and lactation.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Postprandial hormonal response: GLP-1
Timeframe: 24 months (analyzes were performed throughout the study period).
2
Postprandial hormonal response: GIP.
Timeframe: 24 months (analyzes were performed throughout the study period).
3
Postprandial hormonal response: cholecystokinin.
Timeframe: 24 months (analyzes were performed throughout the study period).
4
Postprandial hormonal response: omentin.
Timeframe: 24 months (analyzes were performed throughout the study period).