Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT07268404

Women's Hormonal and Metabolic Wellbeing Study

Led by Daily Nouri · Updated on 2025-12-19

60

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if Daily Nouri Hormone Balance Probiotic blend can improve metabolic, inflammatory, and symptom outcomes in women. Participants will: * Take the probiotic blend or placebo every day for 12 weeks * Complete virtual assessments and report symptoms throughout the study

CONDITIONS

Official Title

Women's Hormonal and Metabolic Wellbeing Study

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-reported irregular menstrual cycles defined by one or more of the following: cycle length usually over 35 days or under 21 days; fewer than 9 menstrual periods in the past year; unpredictable cycle timing varying by more than 7 days month-to-month; irregular cycles present for at least 6 months
  • One or more hormonal balance concerns such as skin issues, unwanted hair growth, hair thinning, or weight concerns
  • Self-reported emotional symptoms that fluctuate with the menstrual cycle including mood swings, irritability, stress, low mood, or difficulty regulating emotions
  • Not currently using hormonal therapies, metformin, GLP-1 receptor agonists, or anti-androgens
  • Willing to stop supplements for menstrual or hormonal support for a 2-week washout before baseline if currently taking any
  • Weight stable within plus or minus 5 pounds for the past 2 months and not planning to start a new diet, exercise program, or medications during the study
  • Able to provide electronic informed consent
  • Willing to complete online surveys and at-home dried blood spot sample collection
  • Negative home pregnancy test at baseline
  • Access to a computer or smartphone and reliable internet connection
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Alethios, Inc.

San Francisco, California, United States, 94109

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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