NCT05875233
Who may be able to join
Who might be able to join this trial:
- You are a woman between 18 and 36 years old.
- You have been diagnosed with polycystic ovary syndrome (PCOS) within the last 5 years.
- You have experienced at least two of the following: irregular or absent periods; excessive facial or body hair, thinning or lost scalp hair, oily skin, or acne; or polycystic ovaries confirmed by an ultrasound scan.
- You are generally healthy and do not have any long-term illness that is uncontrolled or unstable.
- You have concerns about any of the following: irregular periods or ovulation, mood swings, stress, breast tenderness, food cravings, irritability, or low energy.
- You have been following a steady, consistent diet and exercise routine, and are willing to keep that the same for the whole study.
- You are willing to avoid taking any other supplements that could affect your menstrual cycle during the study.
- You are willing and able to follow the study plan, including taking supplements at set times, filling in questionnaires online, and sharing photos where required.
- You are able to communicate in English.
- You are willing to sign a consent form agreeing to take part.
- If joining the hormonal birth control group: you have been using the same hormonal birth control for at least the past 3 months and are willing to keep using it unchanged for the next 6 months.
- If joining the non-hormonal birth control group: you have not used hormonal birth control for the past 3 months, are willing to stay off it for the next 6 months, and experience hormonal or frequent acne breakouts.
Who may not be able to join:
- You have any unstable, uncontrolled, or pre-existing medical or mental health condition.
- You have been diagnosed with any of the following: endometriosis, uterine fibroids, pelvic inflammatory disease, reproductive cancers, chronic liver disease, diverticular disease, colorectal cancer (or a past history of it), chronic pancreatitis, adenomyosis, fibromyalgia, rheumatoid arthritis, lupus, inflammatory bowel disease, chronic uncontrolled migraines, chronic pelvic pain syndrome, multiple sclerosis, or chronic fatigue syndrome.
- You have had your uterus removed (hysterectomy), both ovaries and fallopian tubes removed, or any other gynaecological procedure in the past 6 months.
- You have significant abnormal results from a physical check-up or blood tests, including kidney or liver function levels more than twice the normal range.
- You have a history of severe allergic reactions requiring an epi-pen, or you are allergic to any ingredient in the study supplement.
- You are currently pregnant, breastfeeding, or trying to become pregnant.
- You are unwilling or unable to follow the study plan.
- You are currently using any medication, herbal remedy, or supplement that can affect your menstrual cycle, or you have previously used the products "Elix Daily Harmony" or "Cycle Balance."
- You have started any new medication, supplement, or herbal remedy aimed at weight, skin (acne), mood, or your menstrual cycle within the last 3 months.
- You currently smoke or have smoked in the past 6 months.
- You have a history of substance abuse.
- You regularly drink more than 3 alcoholic drinks per day.
- Your BMI (a measure of body weight relative to height) is over 35.
- If joining the hormonal birth control group: you have changed your hormonal birth control in the past 3 months or plan to change it in the next 6 months.
- If joining the non-hormonal birth control group: you have used hormonal birth control in the past 3 months or plan to start using it in the next 6 months.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Trial details
Where this trial is recruiting
Primary endpoints
To examine the effect of Daily Harmony and Elix Cycle Balance on menstrual cycle regularity and frequency. [Time Frame: Baseline to Week 24]; To examine the effect of Daily Harmony and Elix Cycle Balance on acne as a symptom of hyperandrogenism. [Time Frame: Baseline to Week 24]; To examine the effect of Daily Harmony and Elix Cycle Balance on acne measure via expert skin grading. [Time Frame: Baseline to Week 24]
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.