Gut bacteria may soothe menopause symptoms — a trial puts it to the test

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * To be eligible for inclusion, the Participant must fulfil all the following criteria: 1. Be able to give informed consent. 2. Be between 44 -55 years, inclusive. 3. Experiencing a score of \>4 on all of the symptoms below, within the past 12-months, measured by the MenQoL. 1. sleep disturbances 2. mood changes 3. changes in sexual function 4. Willing to consume the Study Product daily for the duration of the study. 5. Is in general good health, as determined by the investigator. Exclusion Criteria: Participants will be excluded from the study if they meet any of the following criteria: <!-- --> 1. Participants who are pregnant or wish to become pregnant during the study or who are lactating and/or currently breastfeeding. 2. Has food allergies or other issues with foods that would preclude intake of the Study Products or any known severe allergies. 3. Is experiencing surgical menopause (bilateral oophorectomy before natural menopause occurs). 4. Has any significant acute or chronic coexisting health conditions that would prevent them from fulfilling the study requirements, put the Participant at risk or would confound the interpretation of the study results as judged by the investigator on the basis of medical history. Excluded health conditions include: 1. Uterine fibroids (current or previous 12 months) 2. Endometriosis (current or past history) 3. Polycystic ovarian syndrome (current or past history) 4. History of abnormal pap smear (current or previous 12 months) 5. Enema (in the past 12-weeks) 5. Planned invasive medical procedures 3-weeks prior to and for the duration of the study. 6. Current or recent (in the past 4-weeks) use of a medication that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results. Prohibited medications include: 1. Antibiotics 2. Hormone replacement therapies (current or planned use) 3. Hormonal birth control (current or planned use) 4. Laxatives 7. Recent (in the past 12-weeks) initiation of supplements or herbal remedies commonly used to support perimenopause/menopause symptoms. 8. Current or recent (in the past 4-weeks) use of prohibited nutritional or non-nutritional supplements, including: 1. Probiotics 2. Prebiotics 3. Postbiotics 4. Fibre supplements 9. Planned major changes in lifestyle (i.e., diet, dieting, exercise level, travelling) during the duration of the study. 10. Individuals who, in the opinion of the investigator, are considered to be poor attendees or unlikely for any reason to be able to comply with the study. 11. Participants may not be participating in other clinical studies. If the participant has previously taken part in an experimental study, the Investigator must ensure sufficient time has elapsed before entry to this study to ensure the integrity of the results.