N/A
N=13
Evaluation of the Ketogenic Potential of Different Diet Supplements
Healthy Adults
Bottom Line
View on ClinicalTrials.gov: NCT02693106 ↗Enrolled (actual)
13
Serious AEs
0.0%
Results posted
Mar 2020
Primary outcome: Primary: Concentration of Total Plasma Ketones — -18.2; 23; 12.2; 68.5 µmol/L
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Control (Dietary_supplement); Leucine (Dietary_supplement); Butyrate - (Dietary_supplement); Butyrate + (Dietary_supplement); Octanoate - (Dietary_supplement); Octanoate + (Dietary_supplement); Carnitine (Dietary_supplement); Butter fraction (Dietary_supplement)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Université de Sherbrooke
- Primary completion
- Jun 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Concentration of Total Plasma Ketones |
-18.2; 23; 12.2; 68.5; -3.4; 39.7 | — |
Summary
Evaluate the capacity of different dietary supplements to increase ketone production in healthy adults.
Eligibility Criteria
Inclusion Criteria
- Healthy adults aged of 18 years old or older.
- Non-smoking.
Exclusion Criteria
- Diabetes or prediabetes
- Uncontrolled hypertension
- Uncontrolled thyroid function
- Taking medication that will affect lipid/glucose metabolism
- Severe infection or inflammation
- Pregnancy
Data sourced from ClinicalTrials.gov (NCT02693106). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.