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Effect of memantin in treatment of patients with schizophrenia

The comparison effect of memantin in improvement of quality of life and global function in patients with schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014092819320N1
Enrollment
64
Registered
2014-11-01
Start date
2013-07-06
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

schizophrenia. Schizophrenia, schizotypal and delusional disorder

Interventions

Intervention 1: control group:placebo tablet that is similar to memantin in shape,size and color. starting with single dose 5mg per day then increase 5mg each week ,up to 10 mg at morning and 10 mg
Placebo
Treatment - Drugs
control group:placebo tablet that is similar to memantin in shape,size and color. starting with single dose 5mg per day then increase 5mg each week ,up to 10 mg at morning and 10 mg at night after
study group : memantine tab,starting with single dose 5mg per day then increase 5mg each week ,up to 10 mg at morning and 10 mg at night after 4 weeks and continue (10 mg BD)to12 weeks.

Sponsors

Vice chancellor for research of Isfahan Univercity of Medical science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:age group 18-65 ; no mental retardation ;no pregnancy or milking ;diagnosis of schizophrenia for at least 2 years;treatment with atypical anti psychotic from 3 month ago;do not have ECT during 2 week ago Exclusion criteria:allergic to memantin;addiction or dependency to substance or drugs ;other psychiatric disorder or serious neurological deficit.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: at base line,each 4 weeks to 12weeks. Method of measurement: Quality Of Life scale of schizophrenia.;Global Function. Timepoint: at baseline,each 4 weeks to 12weeks. Method of measurement: Global Assesment Of Functioning.;Possitive and negative symptoms. Timepoint: at base line, each 4 weeks to12 weeks. Method of measurement: Possitive And Negative Symptom Scale.;Depression. Timepoint: at base line,each 4 weeks to12 weeks. Method of measurement: Calgary Depressive Scale for Schizophrenia.

Secondary

MeasureTime frame
Side effects. Timepoint: during 12 weeks of study. Method of measurement: history of patient and his/her companion and physical exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadian Sichani Maryam

Isfahan University of Medical Sciences

farshid5@sepahan.iut.ac.ir; Mohammadian99@yahoo.com+98 31 3222 2475

Outcome results

None listed

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