The Effects of Dietary Erythritol on Platelet Reactivity and Vascular Inflammation (NCT05967741)
Randomized Controlled Clinical Trial to Gauge the Effects of Dietary Erythritol on Platelet Reactivity and Vascular Inflammation
🩺 Plain-English Summary (8th-Grade Level)
The purpose is to conduct a dietary intervention study in which human participants will consume beverages sweetened with erythritol or aspartame, each for 2 weeks, in a randomized crossover design
Who can join: Review the eligibility criteria below.
Location: Ragle Human Nutrition Research Center, University of California, Davis — Davis, California
Age range: 18 Years to 70 Years
🧪 Interventions in This Study
- Erythritol (OTHER)
- Aspartame (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Ragle Human Nutrition Research Center, University of California, Davis — Davis, California
📞 Contact the Study Coordinator
Phone: (530) 219-0914
Email: klstanhope@ucdavis.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
Explore by condition: All Platelet Aggregation, Spontaneous clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.