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Negative symptom treatment in schizophrenia disorder

Evaluation of Typical Antipsychotic Augmentation with citalopram in reduction of Negative Symptoms in Inpatient schizophrenia in Ahvaz Golestan Hospital 1389

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138902113843N1
Enrollment
40
Registered
2010-12-01
Start date
2010-08-23
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 disorder. paranoid schizophrenia, hebephrenic schizophrenia, catatonic schizophrenia ,undiffrentiated schizophrenia

Interventions

Intervention 1: citalopram 20mg on the 1st till 7th days, then 40mg on 8th till 42 days. Intervention 2: placebo 1tablet on the 1st till 7th days, then 2 tablets in 8th till 42 days.
Treatment - Drugs
citalopram 20mg on the 1st till 7th days, then 40mg on 8th till 42 days.
placebo 1tablet on the 1st till 7th days, then 2 tablets in 8th till 42 days.

Sponsors

Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Diagnosis of schizophrenia based on DSM-IV TR structured clinical interview by a psychiatrist (faculty member and psychiatry resident), prominent negative Symptoms (PANSS negative score more than 15) , total PANSS score more than 50, no liver disease, no treatment with ECT within 6 months, age between 18 and 70, illness duration at least 1 year. Exclusion criteria: depressive disorder based on DSM-IV TR interview and more than 17 score by Hamilton depression rating scale , MR, schizoaffective, Bipolar disorder, Neurological disorders , severe organic disease for example IHD or CHF, treatment with anti depressants or lithium, deaf mute, substance abuse within 1 month ago (except nicotine and caffeine), use of any other drugs which had interactions with this study, active suicidal or homicidal thoughts, breast feeding or pregnancy, past history of allergy or complications with study medication, EPS, at least 3 months interval with the last dose of long term antipsychotic medication

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Positive symptoms, negative symptoms, general psychopatology. Timepoint: Days 0, 21, and 42. Method of measurement: PANSS scale.

Secondary

MeasureTime frame
Extrapyramidal side effects. Timepoint: Days 0, 21, and 42. Method of measurement: SIMPSON ANGUS SCALE.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Niloufar Khajeddin

Ahvaz Jundishapor University of Medical Sciences

khajeddinn@gmail.com+98 61 1374 3038

Outcome results

None listed

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