400
Participants
Start Date
June 20, 2023
Primary Completion Date
January 1, 2026
Study Completion Date
January 1, 2027
Ketone Supplement
Participants will be given 360mg/kg
Beverage Tolerability Questionnaire (BTQ) and satiety visual analogue scale
Beverage Tolerability Questionnaire (BTQ) and satiety visual analogue scale will be administered at beginning and end of testing day to tests palatability of supplement
Blood Draw
IV cannula will be inserted at the start of Test Day, and removed at the end of Test Day. Blood samples will be collected at 7 timepoints (possibly 1 more). Cannula will be flushed with a small volume of saline after each sample to maintain patency.
Urine Analysis
Prior to consumption of the Study Product, participants will be asked to completely void bladder. And hydration status will be determined via urine specific gravity (USG) reporting \<1.025. Urine passed after the ingestion of the study product will be collected in a plastic container; participants will be asked to void their bladder and collect urine at the end of the test day. The volume produced will be recorded at the end of the study and aliquots will be frozen and stored for future analysis
RECRUITING
The Ohio State University, Columbus
RECRUITING
The Buck Institute, Novato
Collaborators (1)
Buck Institute for Research on Aging
OTHER
Ohio State University
OTHER