Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Dairy Research Institute
With
BioFortis
Provident Clinical Research
Age
20–69
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject is a female or male, 20-69 years of age, inclusive.
Subject has a BMI of 18.5 to 39.9 kg/m2, inclusive.
Subject has resting blood pressure measurements meeting the criteria for pre-hypertension (SBP = 120 to 139 mm Hg and/or DBP = 80 to 89 mm Hg) or stage 1 hypertension (SBP = 140 to 159 mm Hg or DBP = 90 to 99 mm Hg)
Subject reports history of consuming, on average, ≤2 servings/d of dairy foods as part of their normal diet
Subject is willing to consume ≤1 serving/d of dairy foods (other than the study products provided) during each treatment phase.
Subject is willing to maintain a stable body weight and habitual diet and physical activity patterns throughout the trial, with the exception of specific study instructions related to study product intake, alcohol intake, and physical activity.
You may not be if
Subject has known coronary heart disease (CHD) or a CHD risk equivalent
Subject has a history of any major trauma or major surgical event
Subject has digital deformities that would prevent EndoPAT measurements.
Subject has used medications known to alter body weight
Subject has used medications or dietary supplements that, in the opinion of the Investigator, have strong potential to influence blood pressure or endothelial function
Subject has extreme dietary habits (e.g., Atkins diet, very high protein/low carbohydrate).
Clareo Health | Clinical Trial to Assess the Effects of Low-fat Dairy on Systolic Blood Pressure
