Status: Recruiting
JDS-HF3.0 Supplementation on Menopause Related Quality of Life Outcomes in Postmenopausal Women
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.
Participants needed: 250
Trial details
Age: 50-70Biological sex: FemaleType: InterventionalSponsor: Bonafide HealthUpdated: Nov 20, 2025Locations: 1
Eligibility criteria
Healthy biological females who are 50-70 years of age (inclusive). [+8]
Individuals who are lactating, pregnant, or planning to become pregnant during t... [+19]