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Resveratrol in the treatment of chronic schizophrenia

Resveratrol as adjunctive therapy in the treatment of negetive symptoms in patients with schizophrenia: a double blind and placebo controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090117001556N103
Enrollment
60
Registered
2017-12-24
Start date
2018-01-05
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: Intervention group: Tablet Risperidone (4-6 mg/day) combined with 200 mg/day Resveratrol as intervention group for 8 weeks. Intervention 2: Control group: Tablet Risperidone (4-6 mg/d
Treatment - Drugs
Placebo
Intervention group: Tablet Risperidone (4-6 mg/day) combined with 200 mg/day Resveratrol as intervention group for 8 weeks
Control group: Tablet Risperidone (4-6 mg/day) combined with placebo as control group for 8 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Diagnosis of Schizophrenia based on DSM-5 criteria Age between 18-60 Chronic Schizophrenia- duration of the disorder more than 2 years Minimum score of 20 in negative sub score being stable on risperidone( 4 to 6 mg per day) for the last 2 months

Exclusion criteria

Exclusion criteria: Any serious medical or neurological problem IQ less than 70. Substance dependence during the last 6 months(except for nicotine and caffeine) Score on HDRS less than 14 receiving ECT during the last 3 months Acute or chronic systemic diseases History of neurosurgery History of head trauma

Design outcomes

Primary

MeasureTime frame
Severity of schizophrenia. Timepoint: Baseline and weeks 2-4-8 after beginig of treatment. Method of measurement: by Positive and Negative Symptoms Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahin Akhondzadeh

Tehran University of Medical Sciences

s.akhond@sina.tums.ac.ir+98 21 5541 2222

Outcome results

None listed

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