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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01654640
Other study ID # DW_Metformin
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date September 2012
Est. completion date April 2015

Study information

Verified date September 2018
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is the evaluation of effect of metformin on obesity and metabolic disturbance in patients taking clozapine.


Description:

In this study, the investigators are going to examine the effect of metformin on obesity and metabolic disturbance in patients with schizophrenia who have taken clozapine.The metformin 500mg will be administrated per oral twice a day for 24 weeks and for control group, placebo will be given same route and process.


Recruitment information / eligibility

Status Terminated
Enrollment 15
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Age: 18 ~ 65

- Patient with schizophrenia according to DSM-IV criteria

- Patient have signed on the informed consent, and well understood the objective and procedure of this study.

- Patient taking clozapine 3months or more

- Patient increased in weight more than 10 % of that of before antipsychotics use

Exclusion Criteria:

- Patient taking other antipsychotics with clozapine

- Patient in treatment of diabetes

- Patient in treatment of dyslipidemia

- Allergy or hypersensitivity to metformin

- Pregnant or breast-feeding female patient.

- Patient with severe medical condition

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Metformin
metformin 500mg p.o. bid for 24 weeks
Placebo (for metformin)
placebo 1T bid

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital Daewoong Pharmaceutical Co. LTD.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of weight change of weight after 12-week, 24-week. calculation; (weight of 12-week - weight of baseline)/baseline weight (weight of 24-week - weight of baseline)/baseline weight baseline, 12 weeks, 24 weeks
Secondary Positive and Negative Symptom Scale(PANSS) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary MADRS(montgomery asberg depression rating scale) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary Clinical Global Impression-severity(CGI-S) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 6 weeks, 24 weeks
Secondary Clinical Global Impression-improvement(CGI-I) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary Beck's Depression Inventory(BDI) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary Liverpool University Neuroleptic Side Effect Rating Scale(LUNSERS) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary World Health Organization Quality of Life-BREF (WHOQOL-BREF) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary Short form(36) Health survey (SF-36) baseline, 1-week, 4-week, 12-week, 24-week(end-point) baseline, 12 weeks, 24 weeks
Secondary abdominal fat amount CT baseline, 12-week, 24-week baseline, 12 weeks, 24 weeks
Secondary change of prevalence of metabolic syndrome waist circumference, blood pressure cholesterol,triglyceride, HDL-cholesterol,fasting glucose baseline, 12 weeks, 24 weeks
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