Pilot Clinical Trial With Memantine for Cognitive Deficits in Patients With Multiple Sclerosis

Stopped earlyPhase 2MS (type not specified)NCT00638833

What it found

Stopped

The trial ended early for another reason (see below).

Reason given: Unexpected side-effects: reversible and mild to moderate neurological impairment

What was tested

Treatment tested

  • Memantine

Placebo

  • Placebo

What it measured

Main measures

  • to assess the efficacy of Memantine in improving memory deficit in MS patients using the SRT scale

    6 months

    Thinking and memory

Other measures (1)

  • 1. tests for attention (PASAT3, SDMT, Stroop), executive (Raven, MATTIS) and memory (10/36, SRT), quality of life (SF36), and fatigue (Krupp). 2. attention evoked potentials 3. clinical course, disability (EDSS, MSFC, MSSS).

    6 months

    Disability progressionMyelin repairThinking and memoryFatigueQuality of life (reported by participants)

Who could take part

MS (type not specified) · 18 to 65

Show the full criteria

Inclusion criteria

* Patients with MS (McDonald 2002), both sex, age between 18 to 60 years old, all MS subtypes (RR, SP, PP, PR), stable. * Patients with severe cognitive impairment defined as performing 1.5 SD below control group (matched by age and education) in 2 o more subtests based in our previous study (Sepulcre 2006):

Exclusion criteria

* Psychiatric diseases (Cummings) depression (Hamilton >8), drug or alcohol abuse, benzodiazepine therapy or other medical diseases.

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

About this trial

In the sponsor's words

To assess the efficacy of Memantine in improving the cognitive impairment in patients with Multiple Sclerosis (MS)

Papers

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History

    1. Started

      Sept 2007

    2. Main results due

      Mar 2008

    3. Finished

      Mar 2008

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