Trial · NCT02417350
Ketogenic Diet - a Randomized, Controlled, Cross-over Study
NCT02417350, Not applicable, Completed, Umeå University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Ketogenic Diet - a Randomized, Controlled, Cross-over Study. Trials, record NCT02417350. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02417350
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Ketogenic Diet - a Randomized, Controlled, Cross-over Study
- NCT number
- NCT02417350
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 24 participants, actual
- Lead sponsor
- Umeå University
- Conditions
- Healthy
- Interventions
Ketogenic diet for four weeks, then a 15 week washout, and finally a NFA recommended diet for four weeks, NFA recommended diet for four weeks, then a 15 week washout, and finally a ketogenic diet for four weeks.
- First posted
- 2015-04-15
- Last updated
- 2015-11-05
Source ClinicalTrials.gov
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Biomarkers in blood Measured with gaschromatography (GC)-time-of-flight/mass spectrometry (MS) and Bio-Plex Assays | baseline - four weeks | Measured with gaschromatography (GC)-time-of-flight/mass spectrometry (MS) and Bio-Plex Assays |
| Primary | Blood lipids Measured with LipoPrint System | baseline - four weeks | Measured with LipoPrint System |
| Secondary | Body composition Measured with DXA (Dual Energy X-Ray Absorptiometry) | baseline - four weeks | Measured with DXA (Dual Energy X-Ray Absorptiometry) |
| Secondary | Gut microbiota measured with High-throughput sequencing of nucleic acids (DNA/RNA), short-chain fatty acids | baseline - four weeks | High-throughput sequencing of nucleic acids (DNA/RNA), short-chain fatty acids |
| Secondary | Energy substrate utilization during submaximal exercise Measured with indirect calorimetry during ergometer cycling, lactate in blood. | baseline - four weeks | Measured with indirect calorimetry during ergometer cycling, lactate in blood. |
| Secondary | Exercise performance | baseline - four weeks | Cycling at a sub-maximal work rate with increments every 4 min for three periods, thereafter increased work rate every minute until voluntary exhaustion. |
| Secondary | Hand grip endurance | baseline - four weeks | Hand grip test. |
| Secondary | Resting metabolic rate Measured with indirect calorimetry | baseline - four weeks | Measured with indirect calorimetry (Quark RMR, COSMED) |
| Secondary | Hormones Measured with Bio-Plex Assays and ELISA | baseline - four weeks | Measured with Bio-Plex Assays and ELISA |
| Secondary | Cognition Measured with the Stroop color-word test | baseline - four weeks | Measured with the Stroop color-word test |
1 to 10 of 13Source ClinicalTrials.gov
See all 13 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as |
|---|---|
| Stroop Color-Word Test | Secondary outcome |
Source ConductCognition
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02417350
GET https://conductscience.org/api/trials/v1/NCT02417350/registered