Tier 2 — strong
A Randomized, Double-Blind, Placebo-Controlled Trial Comparing the Effects of Commercially Available Ubiquinone, Ubiquinol, and Geranylgeraniol Dietary Supplements on Plasma CoQ10 Concentrations
Journal of Nutrition and Metabolism
2026
2026:5589963
Bibliography
- PubMed
- PMID 42807157
- PubMed Central
- PMC13617315
- Trial registry
- View on ClinicalTrials.gov Registered trial — results not yet published in a peer-reviewed journal.
- Funding
- The trial sponsor listed in the registry is OvationLab. A separate manuscript funding statement was not identified in the accessible publication extracts used for this audit.
- Competing interests
- Christopher R. D'Adamo disclosed service on the Scientific Advisory Board for Designs for Health, Inc.; the other authors declared no conflicts in the article.
Study snapshot
| Design | Randomized, double-blind parallel-arm placebo-controlled trial; registry NCT06640465 lists masking of participant, care provider and outcomes assessor. |
|---|---|
| Model | Healthy adults aged 40 years and older. |
| Sample | 150 randomized; mean age approximately 52.1 years. |
| Intervention | NOW CoQ10 ubiquinone 200 mg/day; Jarrow QH-absorb ubiquinol 200 mg/day; Annatto-GG geranylgeraniol 300 mg/day; Designs for Health CoQnol ubiquinol 200 mg + geranylgeraniol; or placebo. |
| Duration | 8 weeks. |
| Endpoints | Primary: plasma CoQ10 concentration; Lipids; Kidney and liver markers; PROMIS Global Health; POMS-Vigor; SF-36 Vitality; Adverse events |
What the study showed, in plain terms
Key findings
What this study can and cannot tell us
Citation network
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