Completed

Study to Evaluate the Efficacy of Your Super's Moon Balance and Its Impact on Premenstrual Syndrome and Menstrual Symptoms

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Moon Balance

Dietary Supplement
Who is being recruted

Dysmenorrhea+5

+ Menstruation Disturbances

+ Neurologic Manifestations

From 18 to 40 Years
+15 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: February 2022
See protocol details

Summary

Principal SponsorYour Super, INC.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 15, 2022

Actual date on which the first participant was enrolled.

It is hypothesized that the dietary supplement marketed as "YOUR SUPER Moon Balance" will improve subjective wellbeing in trial participants by alleviating common symptoms of PMS and menstrual symptoms, such as pain, cramps, bloating, and lack of energy. Further, the ability of the supplement to reduce biomarkers of inflammation (CRP) and stress (cortisol), and promote sleep, will be evaluated.

Official TitleStudy to Evaluate the Efficacy of Your Super's Moon Balance and Its Impact on Premenstrual Syndrome and Menstrual Symptoms
NCT05237661
Principal SponsorYour Super, INC.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

38 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 40 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

DysmenorrheaMenstruation DisturbancesNeurologic ManifestationsPainPathologic ProcessesSigns and SymptomsPathological Conditions, Signs and SymptomsPelvic Pain

Criteria

10 inclusion criteria required to participate
Individuals with a regular menstruation

Age 18-40

Moderate self-reported discomfort during menstruation-related to bloating, cramps, fatigue, mood swings, or other PMS-related symptoms

Must be in generally good health - no unstable, uncontrolled health condition

Show More Criteria

5 exclusion criteria prevent from participating
Severe chronic conditions, including oncological and psychiatric disorders

Known to have any severe allergic reactions

Currently pregnant, breastfeeding, or wanting to become pregnant for the duration of the study

Participants unwilling to follow the study protocol

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Dietary supplement: Moon Balance

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Citruslabs

Santa Monica, United StatesOpen Citruslabs in Google Maps
CompletedOne Study Center