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Clinical Trial Summary

US residents who have obesity and sign the informed consent form and are screened and enrolled for this study. Participants who are enrolled complete a survey upon enrollment and are randomized into one of two arms. This study is direct to participant and will not utilize clinical sites.


Clinical Trial Description

Participants who meet the eligibility criteria are randomized into any of the two arms including: the placebo arm or the VIOME Precision Nutrition Program (VPNP) arm. Placebo and Viome's Precision Nutrition Program include supplements and/or dietary recommendations towards improving the symptoms associated with metabolic wellness. The trial will last approximately 4 months for each participant. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06190184
Study type Interventional
Source Viome
Contact Mory Mehrtash
Phone (425) 300-6933
Email studies@viome.com
Status Recruiting
Phase N/A
Start date October 26, 2023
Completion date December 31, 2024

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