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The effect of memantine in improving cognitive deficits, quality of life and reducing the negative symptoms in schizophrenic patients.

The effectiveness of memantine in improving cognitive deficits, quality of life and reducing the negative symptoms of schizophrenia patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200918048751N1
Enrollment
40
Registered
2020-10-30
Start date
2020-11-10
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Schizophrenia. Schizophrenia, unspecified

Interventions

Intervention 1: Intervention group: In addition to the routine treatment of schizophrenia (which includes one of the three antipsychotic drugs: clozapine, risperidone, olanzapine), Sobhan Company Mema

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Having diagnostic criteria (DSM-5) for patients with schizophrenia and at least two years after diagnosis Age 18 to 50 years Receive a fixed dose of antipsychotic for at least 8 weeks and for 4 weeks before enrollment Continue treatment with at least one antipsychotic drug during the study

Exclusion criteria

Exclusion criteria: Outstanding neurological or organic disease in clinical and laboratory studies Existence of another axis-based diagnosis (DSM-5) Coexistence with mental retardation Drug addiction or abuse (except nicotine and caffeine) Inability to communicate High risk of suicide Receive ECT in the last two weeks History of memantine sensitivity Having kidney disease Pregnancy and lactation Do not use safe contraception in women

Design outcomes

Primary

MeasureTime frame
Attention of schizophrenic patients. Timepoint: In two time periods before starting the drug and 12 weeks after starting the drug. Method of measurement: Strop computer test.;Executive performance. Timepoint: In two time periods before starting the drug and 12 weeks after starting the drug. Method of measurement: London Tower Computer Test.;Processing speed. Timepoint: In two time periods before starting the drug and 12 weeks after starting the drug. Method of measurement: Strop computer test.

Secondary

MeasureTime frame
Negative symptoms. Timepoint: In the three time periods before, 8 and 12 weeks after the start of the intervention. Method of measurement: Negative Symptoms Assessment Scale.;The quality of life. Timepoint: Three time periods before, 8 and 12 weeks after the start of the intervention. Method of measurement: Specific quality of life questionnaire for schizophrenic patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJoz Qanbari Reyhaneh

Zanjan University of Medical Sciences

reyhane.jozghanbari@gmail.com+98 24 3354 2403

Outcome results

None listed

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