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Memantine in treatment of major depression

A double - blind placebo-controlled trial of memantine added to sertraline in patients with moderate to severe major depression

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201502161556N72
Enrollment
50
Registered
2015-12-08
Start date
2016-01-01
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

Major Depressive disorder. Depressive episode

Interventions

Intervention 1: Tablet serteraline 200 mg/day plus capsule memantine 20mg/day as intervention group for 6 weeks. Intervention 2: Tablet serteraline 200mg/day plus Cap. placebo as control group for 6 w
Treatment - Drugs
Placebo
Tablet serteraline 200 mg/day plus capsule memantine 20mg/day as intervention group for 6 weeks
Tablet serteraline 200mg/day plus Cap. placebo as control group for 6 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: presence of Major Depressive Disorder based on DSM-IV criteria; baseline Hamilton Depression Rating Scale (HAM-D) (17-item) score of at least 22; signing informed consent. Exclusion criteria: presence of psychosis; any diagnosis in Axis I and II; receiving psychotropic medications; receiving any antidepressants during past one month or ECT during past two months; presence of hypo or hyperthyroidism or cardiovascular problems; pregnancy and breast feeding.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Baseline and weeks 2-4-6 after beginig of treatment. Method of measurement: By Hamiltion Depression Rating Scale 17-Item.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shahin Akhondzadeh

Tehran University of Medical Sciences

S.akhond@sina.tums.ac.ir+98 21 6641 8466

Outcome results

None listed

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