Metformin for Treatment of Antipsychotic-induced Dyslipidemia

NCT ID: NCT01778244

Last Updated: 2013-01-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

162 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-11-30

Study Completion Date

2012-06-30

Brief Summary

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Almost all antipsychotics can induce dyslipidemia, but no treatment has been established. Metformin can improve lipid levels in obese patients. The investigators conducted a randomized, placebo-controlled study to test the efficacy of metformin for antipsychotic-induced dyslipidemia.

Detailed Description

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The study was designed as a double-blind randomized controlled trial, with research assessors and patients intended to be blind to the intervention status. The staff members performing the assessment were not involved in implementing any aspect of the intervention.162 patients were randomized to one of two 24-week individual treatments: metformin (1000mg/day)or placebo. Medications were provided in double-blind fashion.The assessments include lipid levels, body weight, body mass index, fasting glucose, fasting insulin and insulin resistance index.

Conditions

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Dyslipidemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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metformin

metformin

Group Type EXPERIMENTAL

metformin

Intervention Type DRUG

1000mg/day for 24 weeks

placebo

placebo

Group Type PLACEBO_COMPARATOR

No interventions assigned to this group

Interventions

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metformin

1000mg/day for 24 weeks

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Diagnostic and Statistical Manual of Mental Disorder-Fourth Edition (DSM-Ⅳ) criteria for schizophrenia dyslipidemia after antipsycotic treatment the duration of illness was less than 12 months taking only one antipsychotic stable outpatient the total score of Positive and Negative Syndrome Scale (PANSS)≤60.

\-

Exclusion Criteria

liver or renal diseases pregnant or lactating women cardiovascular diseases hypertension or diabetes mellitus
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central South University

OTHER

Sponsor Role lead

Responsible Party

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Jingping Zhao

professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Renrong Wu, MD

Role: PRINCIPAL_INVESTIGATOR

Second Xiangya Hospital of Central South University

Locations

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Institute of Mental Health of The Second Xiangya Hospital, Central South University

Changsha, Hunan, China

Site Status

Countries

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China

Other Identifiers

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RRWu

Identifier Type: -

Identifier Source: org_study_id

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