Alternating Hemiplegia of Childhood Clinical Trial
Official title:
"Etude Pilote, Comparative, Monocentrique, randomisée, en Cross Over, en Double Aveugle, Contre Placebo, Testant l'efficacité de l'Huile triheptanoïne Dans Les Hémiplégies Alternantes de l'Enfant" HEMIHEP
The purpose of this project is to study the efficacy of triheptanoin oil in patients with Alternating Hemiplegia of Childhood (AHC) due to ATP1A3 gene mutation.
The clinical spectrum of Alternating Hemiplegia of Childhood (AHC) is wide and characterized
by the association of permanent and paroxysmal (palsy, dystonia, ocular, epileptic,
dysautonomic events) neurological events, with onset in childhood. Most of AHC patients carry
mutations in the ATP1A3 gene. This gene encodes the Na+/K+ ATPase witch is a transmembrane
ion pump generating chemical and electrical gradient of sodium and potassium across the
plasma membrane. Those paroxystic events in AHC patients with mutations in the ATP1A3 gene
could be associated with a glucidic/energetic metabolism or intracerebral excitability
disorder.
Triheptanoin is a triglyceride, whose derivatives pass the blood - brain barrier and enhance
the Krebs cycle functions. Triheptanoin could therefore allow energy supply to the brain,
which is essential for the functioning of the Na+/ K+ ATPase that consumes a significant
amount of energy in the brain.
The investigators goal is to do a pilot study to test the effectiveness on paroxystic
manifestations and the safety of triheptanoin in a small group of patients with Alternating
Hemiplegia of Childhood secondary to ATP1A3 mutations.
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Status | Clinical Trial | Phase | |
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