CClinicalTrials.gg
Status unknownNCT00569764Updated Jun 12, 2009

Effect on Metabolic Parameters of Abilify in SPR

An observational study in Schizophrenia and Metabolic Syndrome, sponsored by Seoul National Hospital. Status unknown at 2 sites in Korea, Republic of. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2009-06-12.

Sponsored by Seoul National Hospital · Observational

The sponsor has not verified this record recently (last verified Jun 2009), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 65 Years
Sex
All
01

Study summary

To measure the long-term changes in weight and plasma lipids after switching antipsychotic treatment to aripiprazole

Read the detailed description

To measure the long-term changes in weight, plasma lipids and fasting blood glucose after switching antipsychotic treatment to aripiprazole, 1 year, open label studies in out and in-patients with schizophrenia.

The measurement of weight and lipid profile and fasting blood glucose will be measured at baseline and every 3 months for 1 year.

02

Conditions studied

  • Schizophrenia
  • Metabolic Syndrome

Keywords

  • schizophrenia
  • metabolic syndrome
  • aripiprazole
03

In context

Metabolic Syndrome

1,963 studies on the registry are indexed under Metabolic Syndrome; 329 are open to participants now.

This study's planned enrollment of 100 is below the median of 200 across 458 observational studies indexed under Metabolic Syndrome.

Browse Metabolic Syndrome studies →

Lead sponsor

Seoul National Hospital is the lead sponsor of 4 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

patients with schizophrenia who want to change an antipsychotics due to metabolic side effects

Inclusion criteria

  • DSM-IV diagnosis with schizophrenia
  • who signed an informed consent

Exclusion criteria

Exclusion Criteria:

  • comorbid with substance abuse or substance dependence
  • pregnancy or lactation
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
100 participants (estimated)
Biospecimen retention
Samples without dna

Groups and cohorts

  • observational

    patients with schizophrenia who want to change an antipsychotics due to metabolic side effect

06

What researchers measure

Primary outcomes

  1. weight lipid profile : HDL, LDL, total-cholesterol, triglyceride fasting blood glucose

    Time frame: 1 year

Secondary outcomes

  1. prolactin ECG

    Time frame: 1 year

07

Study locations

2 of 2 sites recruiting
  • Seoul National Hospital
    Seoul, 039-757, Korea, Republic of
    • Shi Hyun Kang, M.D. · Contact · drshe@hanmail.net · 82-2-2204-0326
    • Jong il Lee, M.D. · Principal investigator
    Recruiting
  • Seoul National Hospital
    Seoul, 139-757, Korea, Republic of
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00569764
Lead sponsor
Seoul National Hospital
Collaborators
Korea Otsuka Pharmaceutical Co., Ltd.
First posted
Dec 7, 2007
Start date
Dec 2007
Completion
Oct 2009 (estimated)
Last update
Jun 12, 2009

Study contacts

Shi Hyun Kang, MD
Contact
drshe@hanmail.net
82-2-2204-0326
Jong-il Lee, M.D.
study director · Seoul National Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2009. You cannot join it, but the record below documents what was studied.

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