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Effects of Memantine on fatigue in patients with Multiple sclerosis

The effect of Memantine on fatigue in patients with Multiple sclerosis: A double-blind randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121231362N1
Enrollment
64
Registered
2017-01-03
Start date
2016-10-31
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis. Multiple sclerosis

Interventions

Intervention 1: Intervention group: memantine, 10 mg oral tablet, one per day for the first week and then twice a day for three months. Intervention 2: Control group: placebo (exactly the same as the
Treatment - Drugs
Intervention group: memantine, 10 mg oral tablet, one per day for the first week and then twice a day for three months
Control group: placebo (exactly the same as the intervention group), oral tablet, one per day for the first week and then twice a day for three months

Sponsors

Iranian Center of Neurological Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: A history of multiple sclerosis (MS) for more than one year; Type of MS was Relapsing Remitting (RR); Subjective fatigue (grade 3 or 4 fatigue based on questionnaires); Age of 20-55 years; Expanded Disability Status Scale (EDSS): 0-5; Consent to participate in the study. Exclusion criteria: Use of Modafinil, Ritalin or Amantadine; A history of seizure and kidney disease; Taking selective serotonin reuptake inhibitors (SSRI); Other types of diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fatigue. Timepoint: before intervention, 3 months after start of intervention. Method of measurement: MFIS Questionnaire.

Secondary

MeasureTime frame
Depression. Timepoint: before intervention, 3 months after start of intervention. Method of measurement: Beck II questionnaire.;Cognitive disorders. Timepoint: before intervention, 3 months after start of intervention. Method of measurement: MACFIMS test.;Disability. Timepoint: before intervention, 3 months after start of intervention. Method of measurement: EDSS test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad hossein Harirchian

Iranian Center of Neurological Research

harirchm@tums.ac.ir+98 21 6694 8899

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026