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Effect of Memantine on epileptic patients

Effects of Memantine on cognitive profile of patients with epilepsy: A randomized, double-blind, placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20121110011424N5
Enrollment
60
Registered
2019-09-25
Start date
2018-08-23
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Epilepsy. Epilepsy and recurrent seizures

Interventions

Intervention 1: Intervention group: 5 mg Memantine oral tablet once a day for 8 weeks and then 10 mg once a day for another 8 weeks with caution. Intervention 2: Control group: placebo once a day for

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients between 15-65 years old Epileptic patients who received anti epileptic drugs over 6 months with mild to moderate cognition impairment Seizure episodes less than four times a month

Exclusion criteria

Exclusion criteria: Progressive neurologic disease, psychiatric disorders, and mental retardation Severe medical illnesses such as renal failure Pregnancy or breast feeding Patients during inter-ictal phase (2 weeks) Patients with seizure episodes more than four times a month adverse drug effect drug allergy or intolerance

Design outcomes

Primary

MeasureTime frame
Cognitive status score according to MMSE (Folstein mini-mental state examination) criteria. Timepoint: Before intervention and 16 weeks after intervention. Method of measurement: Asking questions of MMSE (Folstein mini-mental state examination ).;Cognitive status score according to FAB (Frontal Assessment Battery). Timepoint: Before intervention and 16 weeks after intervention. Method of measurement: Asking questions of FAB (Frontal Assessment Battery).;Cognitive status score according to MoCA (Montreal Cognitive Assessment). Timepoint: Before intervention and 16 weeks after intervention. Method of measurement: Asking questions of MoCA (Montreal Cognitive Assessment).;Adverse events. Timepoint: 16 weeks after intervention. Method of measurement: Adverse events form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Tafakhori

Tehran University of Medical Sciences

a_tafakhori@sina.tums.ac.ir+98 21 6119 0000

Outcome results

None listed

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