Schizophrenia Clinical Trial
Official title:
Phase 4 Study of Metformin on Obesity and Metabolic Disturbance in Patients Taking Clozapine
Verified date | September 2018 |
Source | Seoul National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is the evaluation of effect of metformin on obesity and metabolic disturbance in patients taking clozapine.
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 |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Hospital | Daewoong Pharmaceutical Co. LTD. |
Korea, Republic of,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05039489 -
A Study on the Brain Mechanism of cTBS in Improving Medication-resistant Auditory Hallucinations in Schizophrenia
|
N/A | |
Completed |
NCT05321602 -
Study to Evaluate the PK Profiles of LY03010 in Patients With Schizophrenia or Schizoaffective Disorder
|
Phase 1 | |
Completed |
NCT05111548 -
Brain Stimulation and Cognitive Training - Efficacy
|
N/A | |
Completed |
NCT04503954 -
Efficacy of Chronic Disease Self-management Program in People With Schizophrenia
|
N/A | |
Completed |
NCT02831231 -
Pilot Study Comparing Effects of Xanomeline Alone to Xanomeline Plus Trospium
|
Phase 1 | |
Completed |
NCT05517460 -
The Efficacy of Auricular Acupressure on Improving Constipation Among Residents in Community Rehabilitation Center
|
N/A | |
Completed |
NCT03652974 -
Disturbance of Plasma Cytokine Parameters in Clozapine-Resistant Treatment-Refractory Schizophrenia (CTRS) and Their Association With Combination Therapy
|
Phase 4 | |
Recruiting |
NCT04012684 -
rTMS on Mismatch Negativity of Schizophrenia
|
N/A | |
Recruiting |
NCT04481217 -
Cognitive Factors Mediating the Relationship Between Childhood Trauma and Auditory Hallucinations in Schizophrenia
|
N/A | |
Completed |
NCT00212784 -
Efficacy and Safety of Asenapine Using an Active Control in Subjects With Schizophrenia or Schizoaffective Disorder (25517)(P05935)
|
Phase 3 | |
Completed |
NCT04092686 -
A Clinical Trial That Will Study the Efficacy and Safety of an Investigational Drug in Acutely Psychotic People With Schizophrenia
|
Phase 3 | |
Completed |
NCT01914393 -
Pediatric Open-Label Extension Study
|
Phase 3 | |
Recruiting |
NCT03790345 -
Vitamin B6 and B12 in the Treatment of Movement Disorders Induced by Antipsychotics
|
Phase 2/Phase 3 | |
Recruiting |
NCT05956327 -
Insight Into Hippocampal Neuroplasticity in Schizophrenia by Investigating Molecular Pathways During Physical Training
|
N/A | |
Terminated |
NCT03209778 -
Involuntary Memories Investigation in Schizophrenia
|
N/A | |
Terminated |
NCT03261817 -
A Controlled Study With Remote Web-based Adapted Physical Activity (e-APA) in Psychotic Disorders
|
N/A | |
Completed |
NCT02905604 -
Magnetic Stimulation of the Brain in Schizophrenia or Depression
|
N/A | |
Recruiting |
NCT05542212 -
Intra-cortical Inhibition and Cognitive Deficits in Schizophrenia
|
N/A | |
Completed |
NCT04411979 -
Effects of 12 Weeks Walking on Cognitive Function in Schizophrenia
|
N/A | |
Terminated |
NCT03220438 -
TMS Enhancement of Visual Plasticity in Schizophrenia
|
N/A |