Effects of a Female Hormone Balance Supplement on Symptoms of Polycystic Ovary Syndrome and Severe Premenstrual Syndrome

Rael

Status: Completed

Conditions: Polycystic Ovary Syndrome; Premenstrual Syndrome

Treatments: Dietary Supplement: Female Hormone Balance Supplement

Study type: Interventional

Funder types: Industry

Identifiers

NCT06124300

20336

Details and patient eligibility

About

This is a virtual single group study that will last 12 weeks. Participants will take 1 scoop of the female hormone balance supplement, and mix it with their drink of choice every morning. Questionnaires will be completed at baseline, 1 week, 2 weeks, 4 weeks, and 12 weeks

Enrollment: 40 patients

Sex: Female

Ages: 18 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Women aged between 18 - 55
• BMI less than 35
• Self-reported concerns around irregular menstrual cycles and ovulation, mood swings, stress, irritability, and low energy
• Generally healthy - don't live with any uncontrolled chronic disease
• Self-reported symptoms of PCOS - irregular periods
• Self-reported concerns with hormonal skin issues

Exclusion criteria

• Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
• Anyone with known severe allergic reactions
• Anyone who is pregnant, breastfeeding, or attempting to become pregnant
• Unwilling to follow the study protocol

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

40 participants in 1 patient group

Female Hormone Balance Supplement

Experimental group

Description:

Participants will add 1 scoop of the powder to a drink of choice every morning.

Treatment:

Dietary Supplement: Female Hormone Balance Supplement