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Clinical Trials in Singapore / NCT07136220
Recruiting Observational

A Pilot Study to Evaluate Equol and Its Effects on Menopausal Symptoms Experienced by Women in Singapore

NCT07136220 · tracked via the Priya Life Science Singapore tracker
Sponsor
Ang Seng Bin
Phase
Observational
Started
2025-07-02
Last updated
2025-08-22

Condition(s) studied

Menopause

Investigational drug(s) / intervention(s)

Consumption of soy protein bar

Consumption of soy protein bar: The participants will be provided one soy protein bar to consume after dinner on day 1.

Study summary

The main aim of this study is to evaluate the effect of equol on menopausal symptoms of women. Our hypothesis is that equol producers will have milder menopausal symptoms compared to non-equol producers. Equol is known as a metabolite produced by gut microbiota from soy-related diet and has estrogen-like activity compared to the isoflavones from soybean.

Previous studies have shown that some women can produce equol from soy-related diet, but the others cannot because they don't have the bacteria which can metabolite daidzein in gut even if they take isoflavones thorough soybean products.

This study will involve participants consuming a soy protein bar and collection of urine samples before and after its consumption.

Eligibility

Sex
FEMALE
Min age
40 Years
Max age
60 Years
Healthy volunteers
Accepted
Inclusion Criteria: \- Women aged 40-60 Exclusion Criteria: * Pregnant women * Allergy to Soy * Allergy to nuts * Consumed antibiotics within 7 days of the study * Has a history of autoimmune diseases * Has a history of thyroid disease * On medical treatment with hormone therapy, elective oestrogen receptors modulators * Consuming equol-containing supplements or food * Consuming painkillers * Consuming anti-depressants and/or sleeping pills

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
KK Women's and Children's Hospital Singapore Singapore Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07136220 on ClinicalTrials.gov ↗ ← All trials in Singapore