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Clinical Trial Summary

Patients who are involved in a clinical protocol driven 12 week medical weight loss intervention will be randomized to receive either a placebo or 600 mg of an ashwagandha root extract. The study endpoints are primarily the patients self-reported perception of life stress and sleep quality. The working hypothesis of this study is that the addition of aschwagandha to .the medical weight loss program will improve the self-reported perception of life stress and sleep quality


Clinical Trial Description

During this 12-week medical weight loss program, the randomized patients will also have a baseline measurements and final measurements of blood for selected adipokines , cytokines, and telomerase measurements ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03112824
Study type Interventional
Source Loma Linda University
Contact
Status Completed
Phase N/A
Start date October 5, 2017
Completion date June 23, 2021

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