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The effect of vitamin D addition on treatment response in patients with schizophrenia

The effect of vitamin D addition on treatment response in patients with schizophrenia in zare hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201210163014N6
Enrollment
80
Registered
2013-05-25
Start date
2013-02-28
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. A disorder in which there is an insidious but progressive development of oddities of conduct, inability to meet the demands of society, and decline in total performance. The characteristic negative features of residual schizophrenia (e.g. blunting of affe

Interventions

Intervention 1: In Group A, 600000 IU vitamin D supplementation is added intramuscular to standard atypical antipsychotic drug regimens monthly for three months. Intervention 2: In Group B, as control
Treatment - Drugs
In Group A, 600000 IU vitamin D supplementation is added intramuscular to standard atypical antipsychotic drug regimens monthly for three months.
In Group B, as control group, is received only standard atypical antipsychotic drug regimens. Patients in second group will be supplemented with vitamin D after the 3 months study period.

Sponsors

Vice chancellor for research,Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Schizophrenic patients based on DSM-IV TR criteria ;aged between 18 to 65 years; treated with atypical antipsychotic drugs except clozapine ; Vitamin D deficiency (serum vitamin D concentrations less than 30 ng/ml) . Exclusion criteria: Patients with Acute renal failure; hepatic failure; parathyroid disease and consumption of vitamin D; parathyroid hormone; calcium and phosphorous supplements

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Change in Positive and Negative Syndrome Scale total score (PANSS). Timepoint: Baseline and first,second,third month. Method of measurement: PANSS Questionnaire.

Secondary

MeasureTime frame
Serum vitamin D concentration. Timepoint: Baseline and third month. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Mamashli

Mazandaran University of Medical Sciences

shima.mamashli67@gmail.com+98 15 1354 3083

Outcome results

None listed

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