Trial Outcomes & Findings for Evaluation of the Ketogenic Potential of Different Diet Supplements (NCT NCT02693106)
NCT ID: NCT02693106
Last Updated: 2020-03-25
Results Overview
Difference from Time 0 in Total ketones = acetoacetate (umol/L) + beta-hydroxybutyrate (umol/L) Time 0 is when the participants arrived, after a 12 hours fast, i.e. before the breakfast. Plasma was collected every 30 minutes for 4 hours immediately following breakfast (where supplements were taken). Results are the mean of plasma ketones measured every 30 minutes ( i.e. total of 9 plasma samples) for the 4 hour period. For each time point, the difference form time 0 has been made. So this is the mean of the difference from time 0 in total ketones. Data were not collected for the 'Intervention 8: 65 g of butter fraction rich in MCT' supplement.
COMPLETED
NA
13 participants
4 hours
2020-03-25
Participant Flow
Participant milestones
| Measure |
Ketogenic Potential
Each participant has to go through a total of 8 visits, each visit corresponding to a standardize breakfast taken alone (control visit) or with one of the dietary supplements evaluated followed by a period of 4-hour with multiple blood sampling.
Intervention 1: Control; no supplement Intervention 2: 5 g of leucine Intervention 3: 3.6 g of butyrate Intervention 4: 7.2 g of butyrate Intervention 5: 5 g of octanoate Intervention 6: 10 g of octanoate Intervention 7: 1.95 g of carnitine Intervention 8: 65 g of butter fraction rich in MCT
|
|---|---|
|
Overall Study
STARTED
|
13
|
|
Overall Study
COMPLETED
|
10
|
|
Overall Study
NOT COMPLETED
|
3
|
Reasons for withdrawal
| Measure |
Ketogenic Potential
Each participant has to go through a total of 8 visits, each visit corresponding to a standardize breakfast taken alone (control visit) or with one of the dietary supplements evaluated followed by a period of 4-hour with multiple blood sampling.
Intervention 1: Control; no supplement Intervention 2: 5 g of leucine Intervention 3: 3.6 g of butyrate Intervention 4: 7.2 g of butyrate Intervention 5: 5 g of octanoate Intervention 6: 10 g of octanoate Intervention 7: 1.95 g of carnitine Intervention 8: 65 g of butter fraction rich in MCT
|
|---|---|
|
Overall Study
No time
|
3
|
Baseline Characteristics
Evaluation of the Ketogenic Potential of Different Diet Supplements
Baseline characteristics by cohort
| Measure |
Ketogenic Potential
n=13 Participants
Each participant has to go through a total of 8 visits, each visit corresponding to a standardize breakfast taken alone (control visit) or with one of the dietary supplements evaluated followed by a period of 4-hour with multiple blood sampling.
Intervention 1: Control; no supplement Intervention 2: 5 g of leucine Intervention 3: 3.6 g of butyrate Intervention 4: 7.2 g of butyrate Intervention 5: 5 g of octanoate Intervention 6: 10 g of octanoate Intervention 7: 1.95 g of carnitine Intervention 8: 65 g of butter fraction rich in MCT
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|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
13 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
0 Participants
n=5 Participants
|
|
Age, Continuous
|
34 years
STANDARD_DEVIATION 4 • n=5 Participants
|
|
Sex: Female, Male
Female
|
10 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
3 Participants
n=5 Participants
|
|
Region of Enrollment
Canada
|
13 Participants
n=5 Participants
|
PRIMARY outcome
Timeframe: 4 hoursDifference from Time 0 in Total ketones = acetoacetate (umol/L) + beta-hydroxybutyrate (umol/L) Time 0 is when the participants arrived, after a 12 hours fast, i.e. before the breakfast. Plasma was collected every 30 minutes for 4 hours immediately following breakfast (where supplements were taken). Results are the mean of plasma ketones measured every 30 minutes ( i.e. total of 9 plasma samples) for the 4 hour period. For each time point, the difference form time 0 has been made. So this is the mean of the difference from time 0 in total ketones. Data were not collected for the 'Intervention 8: 65 g of butter fraction rich in MCT' supplement.
Outcome measures
| Measure |
Ketogenic Potential
n=10 Participants
Each participant has to go through a total of 8 visits, each visit corresponding to a standardize breakfast taken alone (control visit) or with one of the dietary supplements evaluated followed by a period of 4-hour with multiple blood sampling.
Intervention 1: Control; no supplement Intervention 2: 5 g of leucine Intervention 3: 3.6 g of butyrate Intervention 4: 7.2 g of butyrate Intervention 5: 5 g of octanoate Intervention 6: 10 g of octanoate Intervention 7: 1.95 g of carnitine Intervention 8: 65 g of butter fraction rich in MCT
|
|---|---|
|
Concentration of Total Plasma Ketones
CTL
|
-18.2 µmol/L
Standard Error 20
|
|
Concentration of Total Plasma Ketones
Leucine
|
23 µmol/L
Standard Error 25
|
|
Concentration of Total Plasma Ketones
Butyrate 3.6g
|
12.2 µmol/L
Standard Error 44.4
|
|
Concentration of Total Plasma Ketones
Butyrate 7.2g
|
68.5 µmol/L
Standard Error 35.9
|
|
Concentration of Total Plasma Ketones
Octanoate 5g
|
-3.4 µmol/L
Standard Error 32.8
|
|
Concentration of Total Plasma Ketones
Octanoate 10 g
|
39.7 µmol/L
Standard Error 34
|
|
Concentration of Total Plasma Ketones
Carnitine
|
-30 µmol/L
Standard Error 21.4
|
Adverse Events
Control, no Supplement
5g of Leucine
3.6g de Butyrate
7.2g de Butyrate
5g d'Octanoate
10g d'Octanoate
1.95g de Carnitine
Serious adverse events
Adverse event data not reported
Other adverse events
| Measure |
Control, no Supplement
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken alone (control visit)followed by a period of 4-hour with multiple blood sampling.
|
5g of Leucine
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken with 5g of leucine followed by a period of 4-hour with multiple blood sampling.
|
3.6g de Butyrate
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken with 3.6g of butyrate followed by a period of 4-hour with multiple blood sampling.
|
7.2g de Butyrate
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken with 7.2g of butyrate followed by a period of 4-hour with multiple blood sampling.
|
5g d'Octanoate
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken with 5g of octanoate followed by a period of 4-hour with multiple blood sampling.
|
10g d'Octanoate
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken with 10g of octanoate followed by a period of 4-hour with multiple blood sampling.
|
1.95g de Carnitine
n=10 participants at risk
Each visit corresponding to a standardize breakfast taken with 1.95g of carnitine followed by a period of 4-hour with multiple blood sampling.
|
|---|---|---|---|---|---|---|---|
|
Gastrointestinal disorders
Diarrhea
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
20.0%
2/10 • Number of events 2 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
20.0%
2/10 • Number of events 2 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
|
General disorders
Headache
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
30.0%
3/10 • Number of events 3 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
|
Gastrointestinal disorders
gastric reflux
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
20.0%
2/10 • Number of events 2 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
30.0%
3/10 • Number of events 3 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
|
General disorders
Nausea
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
20.0%
2/10 • Number of events 2 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
20.0%
2/10 • Number of events 2 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
0.00%
0/10 • 8 visits of 4 hours
no participants received the intervention if 65 g of butter fraction rich in MCT
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place