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A Single Group Study to Evaluate the Effects of a Supplement on Premenstrual Syndrome

Premenstrual Syndrome Clinical Trial

Official title:
A Single Group Study to Evaluate the Effects of a Supplement on Premenstrual Syndrome

Clinical Trial Summary

This is a virtual single-group study that will last three menstrual cycles (approximately 12 weeks). During the first menstrual cycle, participants will take the supplement as needed (pro re nata) when they feel symptoms of PMS, such as cramping or bloating. For the second and third menstrual cycles, Participants will take 2 capsules per day with water for 1 week, starting 4 days before their menstrual cycle and finishing on Day 3 of their cycle. Questionnaires will be completed at the following time points: - Baseline - Day 7 of their first cycle during the trial (After using the product PRN during their period) - 4 days before their second period during the trial (After using the product PRN for the previous month) - Day 3 of their second period during the trial (After using the product for 7 days straight) - Day 3 of their third period of the trial (After using the product for 7 days straight)

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06124326
Study type Interventional
Source Rael
Contact
Status Active, not recruiting
Phase N/A
Start date August 31, 2023
Completion date January 20, 2024
View Details
See also
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