Phase
Condition
Diabetes Prevention
Obesity
Treatment
N/AClinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adults men or women (>18 years old)
Waist circumference ≥102 cm (men) or ≥88 cm (women) and <150cm
Written informed consent provided before the initial screening visit.
Exclusion
Exclusion Criteria:
Use of antibiotics within 30-days period before the study
Waist circumference other than those specified in inclusion criteria
Body mass index (BMI) ≥ 40 kg/m2
Glucose (fasting state) ≥ 126 mg/dL
Anemia (hemoglobin ≤13 g/dL in men and ≤12 g/dL in women)
Suffer from claustrophobia (to the extent that precludes NMR).
Wear pacemakers, electrical stimulators or cochlear implants (NMR contraindications)
Following a hypocaloric diet and/or receiving pharmacologic treatment for weight loss
Having eating disorders.
Use of medication, antioxidant, or multi-vitamin supplements interfering with thestudy
Chronic gastrointestinal pathology
Being intolerant or suffer from allergy to any of the products of the study.
Pregnant or intending to become pregnant
Being in breastfeeding period.
Chronic alcoholism
Current or past participation in a clinical trial or consumption of a research productin the 30 days prior to inclusion in the study.
Failing to follow study guidelines.
Study Design
Study Description
Connect with a study center
Technological Centre of Nutrition and Health (CTNS)
Reus, Tarragona 43204
SpainActive - Recruiting
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