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Riluzole in the treatment of the negative symptoms of schizophrenia

The effect of Riluzole on negative symptoms in patients with chronic schizophrenia: a double blind and placebo controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201107281556N26
Enrollment
30
Registered
2011-07-30
Start date
2011-09-23
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

Interventions

Intervention 1: Tablet Risperidone (2-6 mg/day) combined with 100 mg/day of Tablets Riluzole as intervention group for 8 weeks. Intervention 2: Tablets Risperidone (2-6 mg/day) combined with Tablets p
Treatment - Drugs
Placebo
Tablet Risperidone (2-6 mg/day) combined with 100 mg/day of Tablets Riluzole as intervention group for 8 weeks
Tablets Risperidone (2-6 mg/day) combined with Tablets placebo as control group for 8 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:1- Age between 18-50, 2- Diagnosis of Schizophrenia based on DSM IV 3- chronic Schizophrenia( the duration of the disorder> 2 years), Minimum Score of 60 on Positive and Negative Scale- Exclusion Criteria:1- Substance dependence,2- IQ <70,3-any other mental disorder on axis I, 4-Any serious medical or neurological problem ,5- receiving oral antipsychotic medications during the last week or receiving any depot antipsychotic medication during the last month,6- receiving ECT during the last 14 days,7- hepatic disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Change in the severity of negative symptoms. Timepoint: Baseline and weeks 2, 4, 6 and 8 after begining of treatment. Method of measurement: Positive and Negative Syndrome Scale (PANSS).

Secondary

MeasureTime frame
Change in other PANSS subscale scores. Timepoint: Weeks: 2, 4, 6 and 8. Method of measurement: Positive and Negative Syndrome Scale (PANSS).

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 22, 2026