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Study identifier: NCT07333885 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Impact of Reducose® on Glycemic Response and Menopausal Symptoms in Perimenopausal Women (CALM-R)

Condition: Glycemic Response · Menopause Symptoms  ·  Sponsor: Phynova Group Ltd

PhaseNA
Planned participants120
Who can joinFemale, 40 Years to 60 Years
Healthy volunteersYes

About this study

The purpose of this double-blind, randomized, placebo-controlled trial is to. evaluate daily Reducose® (mulberry leaf extract) supplementation taken with the two largest meals for 12 weeks on improving glycemic response and perimenopausal symptoms in women aged 40-60 years. Glycemic response is measured using Dexcom Stelo continuous glucose monitors during standardized test meals, and menopausal symptoms and sleep/quality-of-life outcomes are assessed using validated surveys administered through the Chloe app in a decentralized U.S. study.

This description comes directly from the study's public registry record.

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Locations (1)

People ScienceLos Angeles, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07333885