A Study of NatureU Burn on Satiety in Healthy Adults (NCT07597382) | Clinical Trial Compass
CompletedNot Applicable
A Study of NatureU Burn on Satiety in Healthy Adults
China14 participantsStarted 2024-04-22
Plain-language summary
This single-center, single-blind, non-randomized crossover exploratory study evaluated the short-term effects of NatureU Burn on postprandial satiety in healthy adults. NatureU Burn is an oral dietary supplement containing Irvingia gabonensis seed extract and high-molecular-weight inulin. Fourteen healthy adults were enrolled, and 12 participants completed the study and were included in the effectiveness analysis. Each participant completed two test sessions separated by at least 48 hours: a reference food session with 75 g medical anhydrous glucose in 250 mL warm purified water and a test food session with one capsule of NatureU Burn plus 75 g glucose in 250 mL warm purified water. Satiety-related questionnaire scores were assessed at fasting baseline and at 30, 60, 90, 120, 180, and 240 minutes after the first bite in each session. The study assessed fullness, hunger, desire for food, and prospective food consumption, and monitored adverse reactions.
Who can participate
Age range
18 Years – 50 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:
* Healthy adults aged 18 to 50 years.
* Male or female participants.
* Body mass index within the normal range of 18.5 to 23.9 kg/m2.
* Regular habit of eating breakfast.
* Able to fast for at least 10 hours after dinner.
* Signed informed consent before enrollment.
Exclusion Criteria:
* Pregnant or breastfeeding women.
* Individuals engaged in heavy physical labor or high-intensity exercise.
* Chronic sleep deprivation during the previous 3 months.
* Self-reported body weight increase or decrease of at least 4 kg during the previous 3 months.
* Current use of weight-loss medications.
* Special dietary patterns, such as low-carbohydrate diet or intermittent fasting.
* Abnormal eating attitude based on eating attitude assessment.
* Serious cardiovascular, hepatic, renal, gastrointestinal, hematologic, or neurologic dysfunction.
* History of bariatric surgery.
* Major surgery or hospitalization within the previous 3 months.
* Eating disorders, including binge eating disorder, anorexia nervosa, or bulimia nervosa.
* Abnormal glucose metabolism or lipid metabolism.
* Intolerance or allergy to the test foods.
* Excessive smoking, defined as more than 15 cigarettes per day.
* Alcohol consumption greater than 15 g alcohol per day.
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
Food-Affected Fullness Score After NatureU Burn Plus Glucose Compared With Glucose Alone
Timeframe: Fasting baseline before food intake and 30, 60, 90, 120, 180, and 240 minutes after the first bite in each test session.