Evaluating how well Cretan carob beverage nutrients are absorbed in healthy adults
Bioavailability of Phenolic Compounds Following the Consumption of a Carob Beverage
This study tests how well healthy men can absorb nutrients from a drink made with Cretan carob powder after following a special diet.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 15 (estimated) |
| Ages | 18 Years and up |
| Sex | Male |
| Sponsor | Harokopio University Academic / other |
| Locations | 1 site (Athens) |
| Trial ID | NCT05870930 on ClinicalTrials.gov |
What this trial studies
This interventional study aims to assess the bioavailability of phenolic compounds from a beverage made with Cretan carob powder in healthy male adults. Participants will follow a low-phytochemical diet for five days before consuming the beverage, after which blood samples will be collected at various time intervals to analyze the absorption of nutrients. The study will involve fifteen healthy male volunteers who meet specific inclusion and exclusion criteria, ensuring a controlled environment for accurate results.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy male adults with normal body fat mass.
Not a fit: Patients with obesity, chronic diseases, or those on specific diets or supplements may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into the health benefits of Cretan carob and its potential role in a healthy diet.
How similar studies have performed: While studies on the bioavailability of various food compounds exist, this specific focus on Cretan carob is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * healthy male adults * normal body fat mass Exclusion Criteria: * obesity (according to body fat mass) * Type 1 Diabetes, cardiovascular diseases, hypertension * thyroid disorder, liver disease, kidney disease * gastrointestinal disease * mental illness * use of nutraceutical supplements or natural products for weight loss * dietitians/nutritionists
Where this trial is running
Athens
- Andriana Kaliora — Athens, Greece (Recruiting)
Study contacts
- Principal investigator: Andriana C Kaliora — Harokopio University of Athens, Greece
- Study coordinator: Andriana C Kaliora
- Email: akaliora@hua.gr
- Phone: +30 6976094521
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.