Memantine for the Treatment of Cognitive Dysfunction and Negative Symptoms in Patients With Chron… (NCT00148616) | Clinical Trial Compass
TerminatedPhase 3
Memantine for the Treatment of Cognitive Dysfunction and Negative Symptoms in Patients With Chronic Schizophrenia
Germany13 participantsStarted 2004-04
Plain-language summary
The purpose of this study is to evaluate the efficacy and safety of 24 weeks memantine add-on treatment to risperidone for the treatment of negative symptomatology and cognitive impairment in patients with chronic schizophrenia.
Who can participate
Age range18 Years – 40 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Diagnosis of schizophrenia (DSM-IV)
* Age 18 to 40
* Stable negative syndrome (PANSS negative score \> 20)
* At least one previous schizophrenic episode
* Informed consent
* Subjects must be considered by the investigator to be compliant with investigations and appointments
* Subjects must have an educational level and a degree of understanding such that they can meaningfully communicate with the investigator
Exclusion Criteria:
* Axis I disorder other than schizophrenia within 12 months, e.g. schizoaffective disorder
* Severe positive symptomatology (PANNS positive score \> PANNS negative score)
* Dependency on alcohol or addictive drugs within 6 months of the baseline evaluation
* Contraindication of risperidone
* Significant neurological, cardiovascular, hepatic, renal, metabolic, or other medical diseases or any clinically relevant abnormalities in laboratory tests
What they're measuring
1
Changes in PANSS negative subscore between memantine and placebo treatment