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adding memantine to treatment of schozopherenia

Adjunctive Memantine Therapy for Negative Symptoms in Schizophrenia: A Double-Blind Placebo Controlled Study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180301038906N1
Enrollment
60
Registered
2018-06-10
Start date
2015-04-01
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

schizopherenia. Schizophrenia

Interventions

Intervention 1: Intervention group: For patients, a daily dose of 5 mg of memantine was started, with a dose of 5 mg a week to reach 20 mg / day (in two doses)..Patients in both groups "had an atypica

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Schizophrenia in the relative recovery period Use of atypical antipsychotics including risperidone and olanzapine No other drugs (except anticholinergic and benzodiazepine) Lack of pregnancy or breastfeeding No serious organic disease and no drug use at the time of entering the study

Exclusion criteria

Exclusion criteria: There is serious organic disease Pregnancy or breastfeeding Existence of dementia

Design outcomes

Primary

MeasureTime frame
The condition of psychotic symptoms. Timepoint: Week 2,4,6. Method of measurement: wechsler.

Secondary

MeasureTime frame
Cognitive and negative symptoms. Timepoint: week 2,4,6. Method of measurement: wechsler.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRaheleh Jahantigh

Mashhad University of Medical Sciences

MohammadzadehA931@mums.ac.ir+98 989157030782

Outcome results

None listed

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