In the present study, muscle perfusion will be studied before and after an oral glucose
challenge following a fasting period.
Other: Beet root
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Full eligibility criteria for NCT01746329
Ages eligible for Study
30 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
Aged 30-70 years.
Obesity (BMI>30 kg/m2)
insulin resistance as fasting glucose levels >6.1 mmol/L.
Reported intense sport activities >10 h/w.
Reported alcohol consumption >28 units/w
Signed Informed consent
Currently not smoking and being a non-smoker for at least 3 months prior to the start of the study.
BMI ≥ 40 kg/m2.
Presence of cardiovascular disease.
Presence of sudden cardiac death in a 1st degree relative at an age <50 years.
Presence of diabetes mellitus type 2.
Regular tea drinker (> 2 cups per day)
All locations for NCT01746329
Radboud University Nijmegen Medical Centre
Nijmegen, Gelderland, Netherlands, 6500 HB
View full eligibility
Tris trial is registered with FDA with number: NCT01746329. The sponsor of the trial is Unilever R&D and it is looking for 18 volunteers for the current phase.
Official trial title: Exploratory Study on the Effect of Nutritional Intervention on Postprandial Skeletal Muscle Microcirculation in Obese Subjects
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