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The effect of added buspiron to atypical antipsychotic drugs in the treatment of negative symptoms in patients with schizophrenia

The effect of added buspiron to atypical antipsychotic drugs in the treatment of negative symptoms in patients with schizophrenia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017010431626N2
Enrollment
40
Registered
2017-03-21
Start date
2017-02-19
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: Patients receive 40 mg buspirone and the second generation antipsychotic equivalent of 2-6 mg of risperidon. Intervention 2: Control group: patients with schizoph
Treatment - Drugs
Placebo
Intervention group: Patients receive 40 mg buspirone and the second generation antipsychotic equivalent of 2-6 mg of risperidon.
Control group: patients with schizophrenia receive 40mg placebo with the second generation of 2-6 mg of risperidone. Placebo pill will be like buspirone about the shape, color, smell and size.

Sponsors

Vice chancellor for research Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Age between 18 and 65 years old; Having schizophrenia according to DSM-VI-TR criteria; Bold negative symptoms( PANSS negative symptom sub-scale score more than 15); Disease duration of more than six months Exclusion criteria: Bipolar disorders; Depression and other psychiatric disorders; Chronic medical conditions (liver, kidney and heart); A history of sensitivity to antipsychotics or buspirone; A history of failure to respond to treatment with adequate doses of antipsychotic medication; History of seizures; Pregnancy; Breastfeeding; Any disruption in the electrocardiogram; Simultaneous treatment with other drugs and active suicidal thoughts

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Negative symptoms. Timepoint: Before intervention, Three and six weeks after intervention. Method of measurement: PANSS questioner.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHatam Boostani

Ahvaz Jundishapur University of Medical Sciences

boostani-h@yahoo.com+98 616133743038

Outcome results

None listed

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