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Trial · NCT02408354

Pilot Study, Comparative, Single-center, Randomized, Crossover, Double-blind, Against Placebo, Testing the Effectiveness of Triheptanoin Oil in Alternating Hemiplegia of Childhood

NCT02408354, Phase 2, Completed, Institut National de la Santé Et de la Recherche Médicale, France

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pilot Study, Comparative, Single-center, Randomized, Crossover, Double-blind, Against Placebo, Testing the Effectiveness of Triheptanoin Oil in Alternating Hemiplegia of Childhood. Trials, record NCT02408354. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02408354

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Pilot Study, Comparative, Single-center, Randomized, Crossover, Double-blind, Against Placebo, Testing the Effectiveness of Triheptanoin Oil in Alternating Hemiplegia of Childhood
NCT number
NCT02408354
Status
Completed
Phases
Phase 2
Enrollment
10 participants, actual
Lead sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Conditions
Alternating Hemiplegia of Childhood
Interventions
Triheptanoin, Placebo
First posted
2015-04-03
Last updated
2025-12-10

Source ClinicalTrials.gov

Registered outcomes7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of neurologic paroxystic events report in patient diary7 monthsvisit 1 at day 0, visit 2 at week 12, visit 3 at week 16, visit 4 at week 28
SecondaryComposite score allying the number of neurological paroxystic events, their duration and severity.7 monthsvisit 1 at day 0, visit 2 at week 12, visit 3 at week 16, visit 4 at week 28
SecondaryClinical Global Impression Scales - Improvement7 monthsvisit 2 at week 12, visit 4 at week 28
SecondaryThe Short Form (36) Health Survey7 monthsvisit 1 at day 0, visit 2 at week 12, visit 3 at week 16, visit 4 at week 28
SecondaryBrain 31phosphorus magnetic resonance spectroscopy7 monthsRatio of Inorganic Phosphate (Pi) over Phosphocreatine during visual stimulation visit 2 at week 12, visit 4 at week 28
SecondaryClinical Safety as measured by questionnaire7 monthsvisit 2 at week 12, visit 4 at week 28
SecondaryBiological Safety as measured by acylcarnitine profile, organic acid dosage7 monthsvisit 2 at week 12, visit 4 at week 28

Outcomes0

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
28969699RESULT

Source PubMed

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.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT02408354

GET https://conductscience.org/api/trials/v1/NCT02408354/registered