Condition: CoQ10 Blood Levels · Sponsor: Midwest Center for Metabolic and Cardiovascular Research
The goal of this clinical trial is to compare the relative bioavailability of coenzyme Q10 (CoQ10) from acute administrations of a CoQ10 product designed for enhanced absorption versus a standard CoQ10 product in healthy men and women. Participants will be asked to come to the clinical on five different occasions, including a screening visit (visit 1, -7 days), two test 1 visits (visits 2 and 3, days 0 and 1), and two test 2 visits (visits 4 and 5, days 7 and 8). During the start of each test visit (visits 2 and 4), the participant will consume each study product with water and a standardized breakfast meal. Then, blood samples will be collected over a 10-hour period, and a standardized lunch, dinner, and snacks will be provided. The participant will return to the clinic the next morning for a blood draw 24 hours after the study product ingestion from the previous day. The same procedures will be repeated 7 to 14 days later with the other study product.
This description comes directly from the study's public registry record.
Caryn Adams, MPH · 6304696600 · cwolfe@mbclinicalresearch.com
Sara Campbell, MPH · 6304696600 · scampbell@mbclinicalresearch.ocm
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| Biofortis Clinical Research | Addison, Illinois, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07530250