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Clinical Trial Summary

The purpose of this project is to study the efficacy of triheptanoin oil in patients with GLUT1 deficiency syndrome.


Clinical Trial Description

The primary objective of the study is: - to evaluate the capacity of triheptanoïn to improve the condition of patients with GLUT1-DS The secondary objectives of the study are: - to confirm the short-term safety of triheptanoïn therapy in patients with GLUT1-DS - to evaluate the short-term effects of triheptanoïn treatment on motor function, autonomy, quality of life and clinical signs of patients with GLUT1-DS - to evaluate the effect of triheptanoïn on brain energy metabolism using non-invasive 31P-MRS spectroscopy after activation of the occipital cortex in order to measure the levels of high-energy phosphates (such as ATP and phosphocreatine) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02014883
Study type Interventional
Source Institut National de la Santé Et de la Recherche Médicale, France
Contact
Status Completed
Phase Phase 2
Start date December 4, 2013
Completion date July 4, 2019

See also
  Status Clinical Trial Phase
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Recruiting NCT05687474 - Baby Detect : Genomic Newborn Screening
Completed NCT04112862 - Sodium Lactate Infusion in GLUT1DS Patients Early Phase 1
Completed NCT02018315 - Treatment Development for Glucose Transporter Type I Deficiency Syndrome (G1D) Phase 1
Withdrawn NCT02021526 - Triheptanoin (C7 Oil), a Food Supplement, for Glucose Transporter Type I Deficiency (G1D) Phase 1/Phase 2
Recruiting NCT02013583 - The Glucose Transporter Type I Deficiency (G1D) Registry
No longer available NCT02018302 - Post Study Continuation of C7 for G1D