Evaluating the Impact of a Multivitamin Supplement to Support Biomarkers Associated With Conception and Pregnancy in Healthy Women
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Healthy Adult Women of Child Bearing Age
- Sponsor
- Perelel Inc.
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Change from baseline (week 0) to end of intervention (week 12) on Serum Folate
- Status
- Completed
- Last Updated
- 11 months ago
Overview
Brief Summary
The goal of this clinical trial is to investigate the effects multivitamin (MVM) on blood biomarkers that are associated with healthy pregnancy and conception in adult women. The main question it aims to answer is:
Is there a significant change in blood biomarkers from baseline (week 0) to end of intervention (week 12) in healthy women consuming multivitamin compared to participants consuming the placebo product?
Participants will:
Take drug MVM or a placebo every day for 12 weeks Visit the clinic at baseline and 12 weeks for serum blood draws and measurements Complete a series of surveys at baseline and 12 weeks
Detailed Description
A 12 week double-blind, placebo-controlled, clinical trial assessing the daily administration of a multivitamin (MVM) or placebo on blood biomarkers associated with healthy pregnancy and conception in healthy adult women. Participants will consume study product or placebo for 12 weeks. Measurements will be taken at baseline and at the end of 12 weeks. Primary Objective: To evaluate in healthy women, the effect of 12-week long daily administration of a multivitamin (MVM) on blood biomarkers associated with healthy pregnancy (Folate). Secondary Objective: To evaluate in healthy women, the effect of 12-week long daily administration of multivitamin (MVM) on blood biomarkers associated with healthy pregnancy * Vitamin B12 * Iron * Omega-3 * Choline * CoQ10
Investigators
Eligibility Criteria
Inclusion Criteria
- •Be able to give written informed consent.
- •Be between 21- 40 years of age (inclusive).
- •Regular menstrual cycles in the past 6 months.
- •Willing to consume the study product daily for the duration of the study.
Exclusion Criteria
- •Participants who are pregnant or wish to become pregnant during the study or who are lactating and/or currently breastfeeding.
- •Participants currently of biological childbearing potential, but not using a continuous effective method of contraception, as outlined below:
- •Complete abstinence from intercourse two weeks prior to administration of the Study Product, throughout the clinical study, until the completion of follow-up procedures or for two weeks following discontinuation of the Study Product in cases where Participant discontinues the study prematurely. (Participants utilizing this method must agree to use an alternate method of contraception if they should become sexually active and will be queried on whether they have been abstinent in the preceding two weeks when they present to the clinic for the final visit).
- •Has a male sexual partner who is surgically sterilised prior to the Screening Visit and is the only male sexual partner for that Participant.
- •Sexual partner(s) is/are exclusively female.
- •Use of acceptable method of contraception, such as a spermicide, mechanical barrier (e.g., male condom, female diaphragm), tubal ligation. The Participant must be using this method for at least one week prior to and one week following the end of the study.
- •Has a history of drug and/or alcohol abuse at the time of enrolment.
- •Is a smoker.
- •Is hypersensitive to any of the contents of the study product, that would preclude intake of the study products.
- •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.
Outcomes
Primary Outcomes
Change from baseline (week 0) to end of intervention (week 12) on Serum Folate
Time Frame: 12 weeks
Secondary Outcomes
- Change from baseline (week 0) to end of intervention (week 12) on Serum Vitamin B12(12 weeks)
- Change from baseline (week 0) to end of intervention (week 12) on Ratio Omega 6: Omega 3 (calculated)(12 weeks)
- Change from baseline (week 0) to end of intervention (week 12) on serum C-Reactive Protein (CRP)(12 weeks)
- Change from baseline (week 0) to end of intervention (week 12) on Serum Iron [including Ferritin, Total Iron Binding Capacity (TIBC) and Transferrin](12 weeks)
- Change from baseline (week 0) to end of intervention (week 12) on plasma Choline(12 weeks)
- Change from baseline (week 0) to end of intervention (week 12) on plasma CoQ10(12 weeks)
- Change from baseline (week 0) to end of intervention (week 12) on RBC Fatty Acid of Omega-3(DHA and EPA) and Omega-6 (CLA and AA)(12 weeks)