This Study Aims to Evaluate Whether Milamend's Product Could Improve Hormone Balance in Women Who Suffer From Self-reported PCOS Symptoms.
Eligible age
18–40 yrs
Accepts
Women
Locations
1 state
Healthy volunteers
No
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About this study
The rationale for this study is to observe the impact of a consumer-grade commercially available product called Milamend Hormone Balance on quality of life and hormonal health in women with self-reported symptoms associated with Polycystic Ovarian Syndrome (PCOS). Additionally, the study aims to observe the impact of the product on menstrual cycle structure and associated symptoms, on reproductive and metabolic markers, on body image concerns, anxiety and general well-being. A consumer-driven, decentralized observational clinical research study is therefore well-suited for examining the effects of this product in this population. We will examine the outcomes in a broad age-range of premenopausal women who have chosen to try this product. The study will incorporate participant reported outcome questionnaires and surveys and at-home blood specimen collection. There is no "doctor-patient" relationship as part of this research since the participant as a consumer is making the informed choice to try the product and take part in the observational process with self-reported measures, cycle tracking and at-home blood sample collection. Findings from this study will contribute knowledge toward the tolerability and formulation of the product and the design of future studies.
Sponsor: Mila Mend Inc.
You may qualify if…
- ✓ 1. Females between 18-40 years old, inclusive
- ✓ 2. Known diagnosis of Polycystic Ovarian Syndrome (PCOS) OR likely have PCOS as defined by presence of:
- ✓ 3. Oligomenorrhea (\<9 menstrual cycles in the past year)
- ✓ 4. Signs of hyperandrogenism (hirsutism, acne, female-pattern hair loss)
- ✓ 5. Has recorded menstrual cycle duration of at least 3 menstrual cycles in the past year
- ✓ 6. BMI of 18.5-35
- ✓ 7. Owns or is willing to purchase a personal digital weight scale for monthly weight measurement.
- ✓ 8. In good general health at the time of screening (Investigator discretion).
You may not qualify if…
- ✕ Any potential participants who:
- ✕ 1. Do not have a personal smartphone, internet access, or unwilling to download Chloe.
- ✕ 2. Rates the impact of PCOS on their overall quality of life as "Rarely/Seldom" or "Not at all"
- ✕ 3. Average cycle length of last 3 cycles is \>50 days
- ✕ 4. Concomitant Therapies:
- ✕ 1. Use of hormonal contraceptives within the last 6 months.
- ✕ 2. Use of a Co-Q10 supplement within the last 6 months.
- ✕ 3. Use of any high dose vitamin B supplements in the last 6 months.
Where it's recruiting
Los Angeles
Source: ClinicalTrials.gov · NCT07764328 · last updated 2026-08-13