Does cerebral hypoperfusion play a role in reduced axonal metabolism and clinical disability in patients with multiple sclerosis ?

CompletedPhase 2Relapsing MS2017-001253-13

What it found

Paper found, not read

A paper reports the results; we have not read it yet. See Papers below.

What it measured

Main measures

  • N-acetyl aspartate (NAA) levels after restoring the cerebral blood flow (CBF) with the endothelin-1 antagonist.

Other measures (1)

  • - Effects on the clinical disability and fatigue in MS patients

    Fatigue

Who could take part

Relapsing MS

Show the full criteria

Inclusion criteria

Inclusion: - Patients with the diagnosis of relapsing-remitting MS, according to the 2010 Revised Mc Donald Criteria Exclusion: - Clinical evidence of MS relapse within 3 months prior to inclusion.

Exclusion criteria

Not separately supplied in the registry.

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

Cerebral perfusion is globally decreased in patients with Multiple Sclerosis (MS) and might contribute to progressive axonal degeneration, cognitive decline and fatigue. In this placebo-controlled, double-blind, randomized trial with the endothelin-1 antagonist bosentan, we want to explore whether pharmacological restoration of cerebral blood flow (CBF) in patients with MS can improve axonal metabolism and clinical disability.

Papers

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History

    1. Started

      Jul 2017

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