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An assessment of effects of melatonin on metabolic effects of olanzapine in patients with schizophrenia

An assessment of effects of melatonin on metabolic effects of olanzapine in patients with schizophrenia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201107187049N1
Enrollment
40
Registered
2011-09-10
Start date
2011-08-06
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, schizotypal and delusional disorders

Interventions

Intervention 1: tablet melatonin 3mg at 9 pm as intervention group. Intervention 2: placebo at 9 pm as contol group.
Placebo
tablet melatonin 3mg at 9 pm as intervention group
placebo at 9 pm as contol group

Sponsors

Guilan University of Medical ScienceS
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: age 18-65 year?diagnosis of schizophrenia based on DSM-IV-TR? capability to take drugs at 9.00 pm Exclusion criteria: married women who are at reproductive age; history of drug abuse or dependence in the recent 30 days;history of taking olanzapine in the recent 3 months;history of allergy or intolerance to olanzapine; history of significant head trauma ( causing loss of concioussness more than 5 minutes or neurolgical or cognitive sequels);liver, kidney, cerebrovascular or cardiovascular disease;diabetes;metabolic syndrome; cancer ;using antiepileptic , antihypertensive or anticoagulant or anti-platelet drugs; using inhibitors or stimulants of hepatic isoenzymes that metabolize melatonin or olanzapine (e.g. omeprazole. rifampin, fluvuxamine, ciprofloxacin, carbamazepine, and modafinil) ; patients develop diabetes; acidosis; severe anticholinergic side effects; delirium or need for administration of another drug

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
TRIGLYCERIDE. Timepoint: baseline,week 4,8,12. Method of measurement: Enzymatic procedure.;Waist cicumference. Timepoint: baseline,week 4,8,12. Method of measurement: with a plastic meter.;Body mass index. Timepoint: baseline,week 4,8,12. Method of measurement: calculated as body weight(kg)divided by the height in meters square.;Waist to hip ratio. Timepoint: baseline,week 4,8,12. Method of measurement: with a plastic meter.;LDL. Timepoint: baseline,week 4,8,12. Method of measurement: Enzymatic procedure.;HDL. Timepoint: baseline,week 4,8,12. Method of measurement: Enzymatic Procedure.;FBS. Timepoint: baseline,week 4,8,12. Method of measurement: Enzymatic Procedure.;Insulin resistance index. Timepoint: baseline and at the end of intervention. Method of measurement: with HOMA formula.;Fasting serum Insulin values. Timepoint: baseline and at the end of intervention. Method of measurement: ELISA.;Blood pressure. Timepoint: baseline,week 4,8,12. Method of measurement: mercury sphygmomanometer.

Secondary

MeasureTime frame
Improvement of sleep problems. Timepoint: base,week 4,8,12. Method of measurement: pittsburgh quality of sleep.;Severity of psychosis. Timepoint: baseline,week 4,8,12. Method of measurement: scale measurement by PANSS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohamadjafar Modabernia

Guilan University of Medical Sciences

jafar_modabbernia@yahoo.com+98 11316662325

Outcome results

None listed

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