Clinical Trials Directory

Trials / Completed

CompletedNCT06124326

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Rael · Industry
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

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)

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPremenstrual Syndrome SupplementGinger, Curcumin, Organic Turmeric, Black Pepper, Magnesium, Zinc, Vitamin B6, Vitamin D.

Timeline

Start date
2023-08-31
Primary completion
2024-01-20
Completion
2024-01-20
First posted
2023-11-09
Last updated
2024-08-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06124326. Inclusion in this directory is not an endorsement.