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A Survey to Evaluate the Cardiovascular Risk Status of Subjects With Pre-Diabetes in Hong Kong (JADE-HK2)
This study is ongoing, but not recruiting participants.
Sponsored by: Chinese University of Hong Kong
Information provided by: Chinese University of Hong Kong
ClinicalTrials.gov Identifier: NCT00786890
  Purpose

Hypothesis: A high cardiovascular risk is present in subjects with pre-diabetes in Hong Kong Chinese.

The investigators plan to assess Chinese subjects in Hong Kong who have pre-diabetes (impaired fasting glucose, IFG; or impaired glucose tolerance, IGT) based on oral glucose tolerance test (OGTT) on their cardiovascular risk status such as obesity, hypertension and lipid profile.


Condition Intervention
Prediabetes
Cardiovascular Risk Factors
Other: observational, no intervention needed

MedlinePlus related topics: Diabetes
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: A Survey to Evaluate the Cardiovascular Risk Status of Subjects With Pre-Diabetes in Hong Kong: The Joint Asia Diabetes Evaluation (JADE) Program Sub-Study 2 (JADE-HK2)

Further study details as provided by Chinese University of Hong Kong:

Primary Outcome Measures:
  • Cardiovascular risk factors: anthroprometric parameters, blood pressure and lipid profiles [ Time Frame: instant ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 3000
Study Start Date: November 2008
Estimated Study Completion Date: January 2014
Estimated Primary Completion Date: November 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
no treatment
observational, no treatment needed
Other: observational, no intervention needed
observational, no intervention needed

  Eligibility

Ages Eligible for Study:   12 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Hong Kong Chinese with pre-diabetes

Criteria

Inclusion Criteria:

  • Hong Kong Chinese with confirmed IFG or IGT by OGTT

Exclusion Criteria:

  • Confirmed diabetic patients
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00786890

Locations
China
Hong Kong Institute of Diabetes and Obesity
Hong Kong, China, HK
Sponsors and Collaborators
Chinese University of Hong Kong
  More Information

Responsible Party: Chinese University of Hong Kong ( Hong Kong Institute of Diabetes and Obesity )
Study ID Numbers: ADF-2008-2
Study First Received: November 5, 2008
Last Updated: November 5, 2008
ClinicalTrials.gov Identifier: NCT00786890  
Health Authority: Hong Kong: Joint CUHK-NTEC Clinical Research Ethics Committee

Keywords provided by Chinese University of Hong Kong:
Prediabetes (IFG, IGT)
Hong Kong Chinese
Cardiovascular risk factors

Study placed in the following topic categories:
Metabolic Diseases
Hyperglycemia
Glucose Intolerance
Prediabetic State
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Metabolic disorder
Glucose Metabolism Disorders

ClinicalTrials.gov processed this record on January 16, 2009