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Acute Pharmacokinetics of Create Wellness Gummies in Healthy Adults
RecruitingHealthy volunteers welcome
Who can join
Ages 18 to 45 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Adults between the ages of 18-45 yrs * Body mass index of \<35 kg/m2 * Recreationally active \[(≥30 minutes of moderate-intensity physical activity per week as defined by the International Physical Activity Questionnaire (IPAQ)\] * Healthy and free from major diseases as determined from screening call and health history questionnaire. * Agrees to complete pre-assessment guidelines (8-hour fast from caloric foods and beverages, 24-hour abstention from vigorous physical activity, caffeine, alcohol, and tobacco). Exclusion Criteria: * Chronic kidney disease, liver disease, chronic obstructive pulmonary disease, or cancer. * Currently using medications that may directly impact the primary outcomes including: diuretics and corticosteroids). * Currently using creatine monohydrate * Severely impaired hearing or speech or inability to speak English.
About the study
The purpose of this study is to compare blood creatine levels following acute oral supplementation of Create Wellness creatine gummies to creatine monohydrate powder.
What is being tested
- Create Wellness Creatine Gummies (dietary supplement)
- Creatine Monohydrate Powder (dietary supplement)
Sponsor: University of Oklahoma · Participants: 16 · Started: 2026-06
Contact the study team
- Sam R. Moore, PhD · Phone: 4053252542
Official record on ClinicalTrials.gov — NCT07579455
Locations in the U.S.
| Oklahoma | ATHENA Laboratory, Norman |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.