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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01811160
Other study ID # INPRF_144
Secondary ID INPRF_144
Status Completed
Phase Phase 4
First received February 28, 2013
Last updated March 12, 2013
Start date October 2008
Est. completion date November 2011

Study information

Verified date March 2013
Source Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente
Contact n/a
Is FDA regulated No
Health authority México: Institutional Review Board at Instituto Nacional de Psiquiatría "Dr. Ramón de la Fuente"
Study type Interventional

Clinical Trial Summary

Schizophrenia and bipolar disorder are frequently associated with an elevated risk for obesity, metabolic syndrome, diabetes mellitus, dyslipidemia and other metabolic disturbances. Second Generation Antipsychotics (SGA) have a demonstrated efficacy in acute and long term treatment of these disorders and are considered a first option on most treatment guidelines. Unfortunately the use of SGA is associated to drug induced weight gain, disturbed glucose and lipid regulation and an increase of cardiovascular risk and mortality as well as non- adherence to treatment. There are several hypotheses attempting to explain the complex pathways that lead to antipsychotic therapeutic effects and their accompanying adverse effects. Recently, in animals receiving SGA, melatonin prevented to a large extent the body weight increase, which indicates a possible role for biological rhythms in SGA induced body weight accumulation. Melatonin is a hormone secreted by the pineal gland that follows a circadian rhythm with an increased secretion in the middle of the night. This hormone acts importantly on the suprachiasmatic nucleus and other areas in the brain and periphery. Thus melatonin is involved in a series of biological functions such as sleep regulation, blood pressure, regulation of circadian rhythms, mood, behavior, and more recently in the regulation of metabolic processes including insulin, leptin, and lipid regulation.

Given previous results in experimental animals, the purpose of the present study is to test the potential effect of melatonin in reducing or preventing some of the metabolic disturbances associated with SGA


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date November 2011
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

1. Men and non-pregnant, non-lactating women aged between 18 and 45 years;

2. DSM-IV-TR criteria for schizophrenia or bipolar disorder type I;

3. free of concomitant medical or neurological illness (as per review of systems and general physical examination);

4. free of DSM-IV current substance abuse or a history of substance dependence in the last six months;

5. who were initiated on continuous treatment with SGA (clozapine, olanzapine, quetiapine or risperidone) for a period no greater than the last three months prior to their inclusion to the present study.

Exclusion Criteria:

1. were diagnosed with hypertension, diabetes mellitus, dyslipidemia, thyroid disorders or hepatic illness;

2. had a history of hypersensitivity to melatonin;

3. exhibited high risk for suicide or high risk for aggressiveness;

4. women who were not practicing reliable forms of contraception. Patients were eliminated from the study if they suspended SGA or two consecutive doses of the study capsule at any point during the follow up period.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Second Generation Antipsychotic Induced Metabolic Adverse Effects

Intervention

Drug:
Melatonin
A capsule of melatonin was administered nightly (20:00hrs).
Placebo
Placebo capsules were administered at 20:00hrs for eight weeks

Locations

Country Name City State
Mexico Instituto Nacional de Psiquiatría "Dr. Ramón de la Fuente" Mexico City México City

Sponsors (1)

Lead Sponsor Collaborator
Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight change Mean change from baseline weight at 8 weeks No
Secondary Mean change in systolic blood pressure Mean change from baseline systolic blood pressure at 8 weeks No
Secondary Mean change diastolic blood pressure Mean change from baseline diastolic blood pressure at 8 weeks No
Secondary Mean change waist circumference Mean change from baseline waist circumference at 8 weeks No
Secondary Mean change hip circumference Mean change from baseline hip circumference at 8 weeks No
Secondary Mean change fat mass Mean change from baseline fat mass at 8 weeks No
Secondary Mean change lean mass Mean change from baseline lean mass at 8 weeks No
Secondary Mean change total body water Mean change from baseline total body water at 8 weeks No
Secondary Mean change glucose Mean change from baseline glucose at 8 weeks No
Secondary Mean change low density lipoprotein Mean change from baseline low density lipoprotein at 8 weeks No
Secondary Mean change high density lipoprotein Mean change from baseline high density lipoprotein at 8 weeks No
Secondary Mean change triglycerides Mean change from baseline triglycerides at 8 weeks No
Secondary Mean change cholesterol Mean change from baseline cholesterol at 8 weeks No
Secondary Mean change Hamilton D scores Mean change from baseline Hamilton D score at 8 weeks No
Secondary Mean change Young Mania rating scale Mean change from baseline Young Mania rating scale at 8 weeks No
Secondary Mean change Positive and Negative Symptoms scale Mean change from baseline Positive and Negative Symptoms scale at 8 weeks No