The Effect Cranberry-Based Products on the Female Microbiome

Launched by OCEAN SPRAY CRANBERRIES, INC. · Jul 31, 2025

Keywords

ClinConnect Summary

This clinical trial is looking at how different cranberry-based products might affect the balance of bacteria in the vagina and gut of generally healthy women before menopause. The study aims to compare the effects of a cranberry product to a placebo (a product without active cranberry ingredients) to see if it can improve gut and vaginal health, as well as how participants feel during the study.

To join the study, women need to be between 18 and 45 years old, have regular menstrual cycles, and be generally healthy with a body weight in a certain range. Participants should not be pregnant or planning to become pregnant during the study and must agree to use birth control if needed. The study will ask participants to follow certain lifestyle guidelines, avoid some foods and supplements like probiotics and high-polyphenol foods (such as berries and dark chocolate), and avoid certain medications during the trial. The study is not yet recruiting, but those interested should be ready to follow these rules and provide health information to help researchers understand the effects of cranberry on women's vaginal and gut health.

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • Pre-menopausal female,
• • 18 - 45 years of age (inclusive) at visit 1.
• • History of regular menstrual cycles (21-35 d per cycle or at the investigator's discretion) for at least 3 months prior to visit 1. Participants that are using contraceptives (IUD, patch, or pills) must be on a stable dose, defined as no change in medication regimen, within 90 days of visit 1 (or within 6 months of visit 1 for copper IUD users) and no plans to change hormonal contraceptive use during the study.
• • BMI ≥18.5 to \<30.0 kg/m2 at visit 1.
• • Willing to adhere to all study procedures, including lifestyle considerations (see section 6.2), and sign forms providing informed consent to participate in the study and authorization to release relevant protected health information to the Clinical Investigator.
• Exclusion Criteria:
• • Women's health related criteria
• • •Female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential and is unwilling to commit to the use of a medically approved form of contraception throughout the study period.
• • General health related criteria
• • Participant has a history or presence of any gastrointestinal condition that could potentially interfere with absorption of the study product (e.g., inflammatory bowel syndrome, celiac disease, history of gastric bypass surgery).
• • History or presence of clinically important cardiac, renal, hepatic, endocrine (including diabetes mellitus), pulmonary, gastrointestinal, biliary, pancreatic, 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 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 •Stable use of hypertension medication is allowed (defined as no change in medication regimen ≤ 90 d of visit 1).
• • Any signs or symptoms of active infection of clinical relevance (e.g., urinary tract or respiratory) within 5 days prior to any test visit. If an infection occurs during the study period, test visits should be rescheduled until all signs and symptoms have resolved and any treatment has been completed at least 5 days prior to testing.
• • History or presence of cancer in the prior 2 years, except for non-melanoma skin cancer.
• • History of any major trauma or major surgical event within 2 months of visit 1.
• • Subject has elective hospitalizations planned (e.g., elective cosmetic procedures) during the study period.
• • Underwent an endoscopy or colonoscopy preparation within 3 months prior to visit 1.
• • Exclusionary products related criteria
• • 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).
• • Use of tobacco/nicotine products (e.g., cigarette smoking, vaping, chewing tobacco) within 12 months of visit 1.
• • Habitual users (i.e., daily or almost daily) of marijuana and hemp products, including CBD products, and willing to abstain from use throughout the study period (topical creams/lotions are allowed). Occasional use (e.g., couple times a month) within 12 months of visit 1 is allowed but requires at least a 14 d washout prior to visit 1 and the participant must be willing to refrain from use during the study.
• • Unstable use of any prescription medication, where stable use is defined as no change in dose or medication type within 90 days of visit 1. This exclusion criterion does not include hormonal contraceptives.
• • Exposed to any non-registered drug product within 30 days prior to visit 1.
• • Antibiotic use within 30 d of visit 1 and throughout the study period.
• • Steroid use within 30 d of visit 1 and throughout the study period.
• • Current habitual user (≥ 3 days/week ≤ 1 month of visit 1) of anti-inflammatory medications (e.g., NSAIDs, acetaminophen, etc.).
• • Use of medications (over-the-counter or prescription) and/or dietary supplements, known to influence GI function, including but not limited to, pre-, post-, and probiotic supplements, fiber supplements, laxatives, enemas, suppositories, H2 blockers, proton pump inhibitors, antacids, anti-diarrheal agents, anti-depressants, and/or anti-spasmodic within 30 d of visit 1 and throughout the study period. Standard multivitamin and mineral supplements are allowed.
• • Willing to avoid consuming probiotics or fermented foods within 14 d of visit 1 and throughout the study period.
• • Willing to avoid consuming high-polyphenol foods and supplements \[e.g., dark colored and polyphenol-rich fruits (berries, grapes, pomegranates, cherries, grapefruit, black currant, plum) and their processed food/juice and related supplement products (e.g. grape seed extract, green tea extract); red wine; dark chocolate; cranberry extract supplements\] throughout the study period.
• • General safety related criteria
• • Known sensitivity, intolerability, or allergy to any of the study products or their excipients.
• • Any condition the 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