Condition: Multiple Sclerosis, Relapsing-Remitting · Sponsor: University Hospital, Strasbourg, France
Centra nervous system (CNF) damage in multiple sclerosis (MS), are mainly attributed to myelin destruction, axonal abnormalities and subsequent degeneration, and are responsible for serious deficiencies. Current therapies are focused on the treatment of inflammation with several types of anti-inflammatory agents. However, there is an urgent need for innovative therapies promoting neuroregeneration and particularly myelin repair. It has been demonstrated that testosterone can act through neural androgen receptors to promote proliferation and differentiation of oligodendrocyte precursors into mature oligodendrocytes in a cuprizone-induced animal model of demyelination. The rare clinical trials on testosterone are mainly exploratory. Here, we sought to demonstrate an effect of testosterone supplementation in testosterone-deficient patients in a multicenter, randomized, parallel-group, double-blind, placebo-controlled phase 2 trial. The main objective will be to determine the neuroprotective and remyelinating effects of testosterone using tensor diffusion imaging techniques and thalamic atrophy analyzes. As secondary objectives, we would like to study the impact of testosterone supplementation on other conventional and unconventional MRI parameters and on clinical outcomes (cognition, fatigue, quality of life, impact on work / activity and anxiety / depression).
This description comes directly from the study's public registry record.
Laurent D KREMER, MD · +333 88 12 87 33 · laurentdaniel.kremer@chru-strasbourg.fr
Nicolas COLLONGUES, MD · +333 88 12 87 33 · nicolas.collongues@chru-strasbourg.fr
Always discuss trial participation with your own doctor first.
| CHU de Besançon | Besançon, France | Recruiting |
| CHU Nancy | Nancy, France | Recruiting |
| Hôpital Pitié-Salpêtrière | Paris, France | Recruiting |
| CHU de Rennes/Pontchaillou | Rennes, France | Recruiting |
| CHRU de Strasbourg | Strasbourg, France | Recruiting |
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Source record: clinicaltrials.gov/study/NCT03910738