Skip to content

Raloxifene in the treatment of schizophrenia

The effect of raloxifene in postmenopausal women with chronic schizophrenia: a randomized double blind and placebo controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205131556N42
Enrollment
46
Registered
2012-05-13
Start date
2012-06-21
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

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Postmenopausal women, Diagnosis of Schizophrenia based on DSM IV , chronic Schizophrenia( duration of the disorder>2 years), Minimum Score of 20 on Negative subscale Exclusion Criteria: Substance dependence( except for nicotine and cafeine), IQ <70, any other mental disorder on axis I, Any serious medical or neurological problem , receiving oral antipsychotic medications during the last week or receiving any depot antipsychotic medication during the last month, receiving ECT during the last 14 days,hepatic and renal disease , Endocrine abnormality, history of thrombosis and emboli, history of abnormal uterine bleeding, uterine or breast cancer, history of CVA, Hormone replacement therapy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of schizophrenia. Timepoint: Baseline and weeks 2-4-6-8 after beginig of treatment. Method of measurement: Positive and Negative Syndrome Scale (PANSS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactProf. 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: Mar 20, 2026