Can a cooking oil protect the brain in Huntington's?
NCT ID NCT02453061
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special oil called triheptanoin can slow brain damage in people with early Huntington's disease. 100 participants took either the oil or a placebo for 6 months, followed by 6 months where everyone got the oil. The main goal was to see if it reduced brain shrinkage and improved energy use in the brain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Triheptanoin oil
- What this could lead to
- If it works, this could point toward a treatment that slows brain damage and delays symptoms in Huntington's disease.
- What could go wrong
- This is a small, early-phase study (Phase 2) with only 100 people. The results may not show clear benefit, and the oil could cause side effects like stomach upset.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
100 people
The number who actually took part.
- Started
-
Jun 2015
- Finished
-
Dec 2019
- Lead sponsor
-
A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Positive genetic test with CAG repeat length ≥39 in HTT gene * At least 18 years of age * Signature of informed consent * Covered by social security * UHDRS score between 5 and 40 * Ability to undergo MRI scanning * BMI between 18 and 30 Exclusion Criteria: * Hypersensitivity to triheptanoin or to one of its excipients * Additional major comorbidities * History of severe head injury * Participation in another therapeutic trial (3 month exclusion period) * For women of childbearing age, the absence of two forms of effective contraception (with the exception of those who are abstinent) * Pregnancy or breastfeeding * Inability to understand information about the protocol * Persons deprived of their liberty by judicial or administrative decision * Adult subject under legal protection or unable to consent * Treatment with tetrabenazine
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Department of Neurology
Leiden, 2300RC, Netherlands
-
Département de Génétique
Paris, 75013, France
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