An Investigation of Premama Balance and Its Effects on Hormonal Imbalances

Premama

Status: Withdrawn

Conditions: Menstrual Irregularity; Menstrual Pain; Hormone Disturbance; PMS; Menstrual Discomfort

Treatments: Dietary Supplement: PreMama Balance; Dietary Supplement: Placebo Drink

Study type: Interventional

Funder types: Industry

Identifiers

NCT05518006

20223

Details and patient eligibility

About

An investigation of the dietary supplement marketed as "Premama Balance" on markers of subjective wellbeing in trial participants such as common symptoms of PMS and menstrual symptoms, as well as its effects on aiding in returning to their perceived regular/normal menstrual cycle.

Sex: Female

Ages: 20 to 42 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Must be in good health (don't report any medical conditions asked in the screening questionnaire)
• Must be on hormonal birth control (containing both progesterone and estrogen) for the past 6 months & willing to stop using it to participate in the study
• Must be willing to get off of hormonal birth control for the study period
• Must be able to track their menstrual cycle
• BMI under 40
• Agree to refrain from any lifestyle changes that may affect their menstrual cycle for the duration of the study
• Willingness to adhere to the dietary supplement regimen
• Willingness to refrain from any other dietary supplements targeting the menstrual cycle and hormone control during the study period
• Is able to communicate in English
• Is willing and able to share feedback via the used technology portal
• Must provide written informed consent (ICF)

Exclusion criteria

• History of oncological (including ovarian cancer) or psychiatric conditions
• History of uncontrolled health conditions
• History of hysterectomy or ovariectomy
• History of diabetes & thyroid disorders
• Smoker
• More than 3 servings of alcohol a day
• Undergoing hormonal therapy of any kind
• Menopausal or peri-menopausal
• Not starting any other form of contraceptive other than condoms, abstinence, planned sexual intercourse
• Usage of any medication or herbal remedies/supplements which can affect the menstrual cycle or hormonal balance
• If currently taking allowed supplements, the dosage needs to remain the same throughout the entirety of the study

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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0 participants in 2 patient groups, including a placebo group

PreMama Balance

Experimental group

Description:

Each day, the participants will take 1 packet of Premama Balance, dissolved in one glass (8oz+) of water. Premama Balance may be taken with or without food. Should participants present themselves with a sensitive stomach, it is recommended to take the drink with or after a meal to avoid an upset stomach. Participants will repeat this process daily for 6 months/24 weeks (study period) until the study is complete. At week 12 and in week 24, the participants will take a survey and a hormone test to track progress. In total there will be 3 surveys and 3 hormone tests. Additionally, participants will fill out a weekly consumption survey to track compliance.

Treatment:

Dietary Supplement: PreMama Balance

Placebo Drink

Placebo Comparator group

Description:

Each day, the participants will take 1 packet of Placebo Drink, dissolved in one glass (8oz+) of water. Placebo Drink may be taken with or without food. Should participants present themselves with a sensitive stomach, it is recommended to take the drink with or after a meal to avoid an upset stomach. Participants will repeat this process daily for 6 months/24 weeks (study period) until the study is complete. At week 12 and in week 24, the participants will take a survey and a hormone test to track progress. In total there will be 3 surveys and 3 hormone tests. Additionally, participants will fill out a weekly consumption survey to track compliance.

Treatment:

Dietary Supplement: Placebo Drink