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Study identifier: NCT07238478 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

JDS-HF3.0 Supplementation on Menopause Related Quality of Life Outcomes in Postmenopausal Women

Condition: Joint Discomfort · Joint Pain, Stiffness, Function · Joint Pain  ·  Sponsor: Bonafide Health

PhaseNA
Planned participants250
Who can joinFemale, 50 Years to 70 Years
Healthy volunteersYes

About this study

The goal of this interventional study is to evaluate whether the study product can help improve quality of life and reduce common menopause symptoms-such as joint discomfort, hot flashes and night sweats-in women aged 50-70. The primary research question is whether taking the study product daily for 12 weeks can reduce the severity and frequency of menopause-related symptoms.

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

Talk to the study team

Trisha VanDusseldorp, PhD  ·  233-266-2343  ·  tvandusseldorp@bonafidehealth.com

Always discuss trial participation with your own doctor first.

Locations (1)

Bonafide HealthHarrison, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07238478