Postprandial Response to Fruit Juice
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-45
SponsorOcean Spray Cranberries, Inc.
About this trial
The goal of this clinical trial is to determine postprandial responses to fruit juices.
Eligibility criteria
Qualifiers
≥18 to ≤45 years of age at Visit 1.
BMI ≥18.5 and <30.0 kg/m2 at Visit 1.
Fasting capillary glucose ≤110 mg/dL at Visit 1.
Willing to avoid consuming high-polyphenol containing foods for 48 hours prior to each test visit.
Disqualifiers
History or presence of clinically important cardiac, renal, hepatic, endocrine, pulmonary, biliary, pancreatic, gastrointestinal, or neurological disorders that may affect the participant's ability to adhere to the study protocol and/or affect study outcomes, in the judgment of the Clinical Investigator.
Uncontrolled hypertension (systolic blood pressure ≥140 mm Hg or diastolic blood pressure ≥90 mm Hg) as defined by the blood pressure measured at Visit 1 (Section 9.1.1).
Unstable use (initiation or change in dose) within 30 days of Visit 1 of antihypertensive medications.
Unstable use (initiation or change in dose) within 30 days of Visit 1 of thyroid hormone replacement medications.
Trial design
Treatments tested in this trial
- Beverage 1
- Beverage 2
- Beverage 3
- Beverage 4
- Beverage 5
- Beverage 6
Treatment groups
18 Participants
are divided into 6 treatment groups6
Treatment groupsSee each treatment group below.
Sponsors and collaborators
Ocean Spray Cranberries, Inc.
Lead sponsor
Biofortis Innovation Services
Collaborator
Source ClinicalTrials.gov