| NCT ID | NCT07103083 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ocean Spray Cranberries, Inc. |
| Condition | Blood Glucose |
| Study Type | INTERVENTIONAL |
| Enrollment | 18 participants |
| Start Date | 2025-07-21 |
| Primary Completion | 2025-09-26 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 18 participants in total. It began in 2025-07-21 with a primary completion date of 2025-09-26.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this clinical trial is to determine postprandial responses to fruit juices.
Eligibility Criteria
Inclusion Criteria: 1. ≥18 to ≤45 years of age at Visit 1. 2. BMI ≥18.5 and \<30.0 kg/m2 at Visit 1. 3. Fasting capillary glucose ≤110 mg/dL at Visit 1. 4. Willing to avoid consuming high-polyphenol containing foods for 48 hours prior to each test visit. 5. Willing to abstain from alcohol consumption for 24 hours prior to each study visit. 6. Non-user of tobacco or nicotine products (e.g., cigarette smoking, vaping, chewing tobacco) within 12 months of Visit 1, with no plans to begin use during the study period. 7. Non-habitual users (i.e., daily or almost daily) of marijuana or hemp products, including Cannabidiol (CBD)/Tetrahydrocannabinol (THC) products, and willing to abstain from use throughout the study period (topical creams/lotions are allowed). 8. Willing to maintain habitual physical activity level throughout the duration of the study. 9. Willing to maintain habitual dietary pattern throughout the duration of the study, including stable intake of current vitamins, minerals, supplements and medications not interfering with study outcomes. 10. Score of 7 to 10 on the Vein Access Scale at Visit 1. 11. No health conditions that would prevent him/her from fulfilling the study requirements as judged by the Clinical Investigator on the basis of medical history. 12. Understands the study procedures and signs forms providing informed consent to participate in the study and authorizes the release of relevant protected health information to the Clinical Investigator. Exclusion Criteria: 1. 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. 2. 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). 3. Unstable use (initiation or change in dose) within 30 days of Visit 1 of antihypertensive medications. 4. Unstable use (initiation or change in dose) within 30 days of Visit 1 of thyroid hormone replacement medications. 5. Use of medications or supplements that may influence carbohydrate metabolism within 30 days of Visit 1. 6. Extreme dietary habits (e.g., ketogenic, very high protein, very high fiber, vegan, vegetarian) at the discretion of the Clinical Investigator. 7. Weight loss or gain \>4.5 kg in the 60 days prior to Visit 1. 8. Currently, or planning to be, on a weight loss regimen during the study. 9. Use of weight loss medication within 90 days of Visit 1. 10. History of gastrointestinal surgery for weight reducing purposes. 11. History of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, or binge eating) diagnosed by a health professional. 12. Known allergy or sensitivity to any ingredients or potential allergens contained in the study beverages. 13. History or presence of cancer in the prior 2 years, except for non-melanoma skin cancer. 14. History of any major trauma or major surgical event within 60 days of Visit 1. 15. Blood donation \>450 mL within 60 days of Visit 2 or plans to donate blood or plasma during the study period. 16. Female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential with unstable use (initiation or change in dose) within 30 days of Visit 1) of sex hormones for contraception. 17. Recent history of (within 12 months of screening; Visit 1) or strong potential for alcohol or substance abuse. Alcohol abuse is defined as \>14 drinks per week (1 drink = 12 oz beer, 5 oz wine, or 1½ oz distilled spirits). 18. Exposed to any non-registered drug product within 30 days prior to Visit 1. 19. Any condition the Clinical Investigator believes would interfere with the participant's ability to provide informed consent or comply with the study protocol, which might confound the interpretation of the study results or put the person at undue risk.
Contact & Investigator
Elizabeth Antoo, MD
PRINCIPAL INVESTIGATOR
Biofortis Innovation Services
Frequently Asked Questions
Who can join the NCT07103083 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 45 Years, studying Blood Glucose. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07103083 currently recruiting?
Yes, NCT07103083 is actively recruiting participants. Contact the research team at ksmith@oceanspray.com for enrollment information.
Where is the NCT07103083 trial being conducted?
This trial is being conducted at Addison, United States.
Who is sponsoring the NCT07103083 clinical trial?
NCT07103083 is sponsored by Ocean Spray Cranberries, Inc.. The principal investigator is Elizabeth Antoo, MD at Biofortis Innovation Services. The trial plans to enroll 18 participants.