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The effectiveness of adding modafinil drug on negative symptoms of schizophrenic patients

The effectiveness of adding modafinil drug on negative symptoms of schizophrenic patients being treated with risperidone or olanzapine

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161228031626N6
Enrollment
42
Registered
2023-07-15
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-07-25

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: In this group, patients will receive 100 to 200 mg of modafinil per day for 4 weeks in addition to the prescribed antipsychotic treatment (resperidone or olanzapine

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with schizophrenia based on DSM-5 criteria Schizophrenic patients who have been treated with risperidone or olanzapine.

Exclusion criteria

Exclusion criteria: Taking typical antipsychotic and atypical antipsychotic drugs, except for risperidone and olanzapine, and antidepressants, sodium valproate, lithium, and benzodiazepines. The presence of accompanying psychiatric disorders such as schizoaffective or other psychotic disorders, bipolar disorder, anxiety disorders such as panic disorder or obsessive-compulsive disorder, post-traumatic stress disorder, eating disorder Dependence or abuse of substances, drugs or alcohol, acutely or in the past 12 months, except for nicotine Allergy to Modafinil or any of the placebo ingredients

Design outcomes

Primary

MeasureTime frame
Negative symptoms. Timepoint: Before and 4 weeks after the study. Method of measurement: Scale for Assessment of Negative Symptoms (SANS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHatam Boostani

Ahvaz University of Medical Sciences

boostani-h@ajums.ac.ir+98 61 3374 3001

Outcome results

None listed

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