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COMPLETED NA

Effects of a Female Hormone Balance Supplement on Premenstrual Syndrome Symptoms

NCT07018479 · View on ClinicalTrials.gov ↗

Study Summary

This virtual single-group study evaluates the effects of the FemmeBalance supplement on symptoms of premenstrual syndrome (PMS) over four menstrual cycles. The study involves daily intake of the supplement, regular questionnaires, and skin photo submissions for dermatological grading.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT FemmeBalance Supplement Group

Study Locations (1)

Nevada

  • Citruslabs — Las Vegas

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2024-07-30
Est. Completion 2025-01-20
Phase NA

Sponsor

VINABAS FORMULATIONS SL

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07018479

The ClinicalTrials.gov registry entry for NCT07018479 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is VINABAS FORMULATIONS SL, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Premenstrual Syndrome appearing as the primary indexed condition, and to 1 intervention — of which FemmeBalance Supplement Group is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07018479 reports 1 study location spanning 1 distinct geographic area — top geographies include Nevada. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07018479 about?

NCT07018479 is a clinical study titled "Effects of a Female Hormone Balance Supplement on Premenstrual Syndrome Symptoms". This virtual single-group study evaluates the effects of the FemmeBalance supplement on symptoms of premenstrual syndrome (PMS) over four menstrual cycles. The study involves daily intake of the supplement, regular questionnaires, and skin photo submissions for dermatological grading.

What is the current status of trial NCT07018479?

This trial is currently completed. It is a NA study. The enrollment target is 38 participants. The study started on 2024-07-30. Estimated completion is 2025-01-20.

What conditions does trial NCT07018479 study?

This clinical trial studies the following conditions: Premenstrual Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07018479?

The interventions under investigation include: FemmeBalance Supplement Group (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07018479?

This trial is sponsored by VINABAS FORMULATIONS SL, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07018479 being conducted?

This trial has 1 study location across Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial