- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02640859
Investigation of Metabolic Risk in Korean Adults
March 14, 2019 updated by: Soo Lim, Seoul National University Bundang Hospital
A cohort study with Korean adults to investigate biomarkers in prediction of cardiometabolic and other diseases
Study Overview
Status
Completed
Conditions
Detailed Description
This is a prospective cohort study with Korean adults to investigate biomarkers in prediction of cardiometabolic and other diseases
Study Type
Observational
Enrollment (Actual)
1003
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Gyeonggi
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Seongnam, Gyeonggi, Korea, Republic of, 463-707
- Seoul National University Bundang Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Healthy Korean Adults
Description
Inclusion Criteria:
- Healthy adults without chronic diseases
- Diabetic patients who are well controlled with oral antidiabetic agents
- Hypertensive patients who are well controlled with oral antihypertensive agents
- Dyslipidemic patients who are well controlled with oral lipid-lowering agents
Exclusion Criteria:
- Malignancy
- Chronic wasting disease
- Long-term steroid use
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Normal cohort
Normal cohort for biobank
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of cardiovascular disease
Time Frame: 5 years
|
5 years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of diabetes mellitus
Time Frame: 5 years
|
5 years
|
Incidence of fatty liver
Time Frame: 5 years
|
5 years
|
Incidence of metabolic syndrome
Time Frame: 5 years
|
5 years
|
Incidence of osteoporosis
Time Frame: 5 years
|
5 years
|
Incidence of sarcopenia
Time Frame: 5 years
|
5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Soo Lim, MD, PhD, SNUBH
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2015
Primary Completion (Actual)
November 30, 2018
Study Completion (Actual)
February 28, 2019
Study Registration Dates
First Submitted
December 19, 2015
First Submitted That Met QC Criteria
December 22, 2015
First Posted (Estimate)
December 29, 2015
Study Record Updates
Last Update Posted (Actual)
March 15, 2019
Last Update Submitted That Met QC Criteria
March 14, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SNUBH-Biobank
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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