Acute Pharmacokinetics of Create Wellness Gummies in Healthy Adults (NCT07579455) | Clinical Trial Compass
RecruitingNot Applicable
Acute Pharmacokinetics of Create Wellness Gummies in Healthy Adults
United States16 participantsStarted 2026-06
Plain-language summary
The purpose of this study is to compare blood creatine levels following acute oral supplementation of Create Wellness creatine gummies to creatine monohydrate powder.
Who can participate
Age range
18 Years – 45 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Peak plasma concentration (Cmax)
Timeframe: 0 to 5-hours following supplementation.
2
Time to peak plasma concentration (Tmax)
Timeframe: 0 to 5-hours following supplementation.
3
Area under the curve (AUC)
Timeframe: 0 to 5-hours following supplementation.