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Ropinirole for the treatment of schizophrenia

The effect of Ropinirole as an adjuvant therapy on the improvement of negative symptoms in patients with chronic schizophrenia: A randomized, double-blind, placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090117001556N165
Enrollment
50
Registered
2025-08-16
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-08-19

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: ?Control group: Patients treated with risperidone (Poursina co.) at a dose of 4-6 mg along with placebo. The chemical formula of risperidone is C23H27FN4O2, which is administered orall

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 Age between 18-60 At least 2 years have been passed since the diagnosis Treated with risperidone for at least 2 months (4-6mg)

Exclusion criteria

Exclusion criteria: Head trauma History of shock therapy during the last three months Neurosurgery Diagnosis of acute or chronic systemic disease Alcohol or drug addiction in the last 6 months Suicidal ideation Pregnancy or lactation IQ less than 70 based on the diagnosis of a psychiatrist Depressive symptoms and use of antidepressants

Design outcomes

Primary

MeasureTime frame
Severity of schizophrenia. Timepoint: Baseline and weeks 4 and 8. In the present study, the severity of negative symptoms will be evaluated at day 0, 4 weeks after treatment, and 8 weeks after treatment. Method of measurement: By Positive and Negative Syndrome Scale (PANSS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shahin 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