Epidemiologic Study to Evaluate the Proportion of Cardiovascular Disease Risk Factors in Korean Hypertensive Patients
WONDeR
A Multi-center, Observational, Cross-sectional Study to Evaluate CVD Risk Factors in Korean Hypertensive Patients
1 other identifier
observational
3,109
0 countries
N/A
Brief Summary
The purpose of this study is investigating the proportion of Cardiovascular disease risk factors of hypertensive patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2010
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2011
CompletedFirst Submitted
Initial submission to the registry
May 5, 2011
CompletedFirst Posted
Study publicly available on registry
May 30, 2011
CompletedDecember 1, 2016
November 1, 2016
5 months
May 5, 2011
November 30, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
Proportion of patients with cardiovascular disease high risk factors
Between patients with essential hypertension
6years, average duration of hypertension
Secondary Outcomes (3)
Proportion of patients with Cardiovascular disease risk factors
6years, average duration of hypertension
Proportion of patients with Cardiovascular disease
6years, average duration of hypertension
Target Blood Pressure achievement rate according to the proportion of Cardiovascular disease risks
6years, average duration of hypertension
Study Arms (1)
Hypertension
Subject who meet eligible criteria
Interventions
Blood sampling for Fasting Plasma Glucose, Hemoglobin A1C, Cholesterols, Blood Urea Nitrogen, Creatinine
Eligibility Criteria
Korea, Diagnosed hypertensive patient
You may qualify if:
- Essential hypertensive patient no less than 18 yeas old
- Patient who gave informed consent form
You may not qualify if:
- Patient was diagnosed as secondary hypertension
- Patient who have white-coat hypertension
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- GlaxoSmithKlinelead
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
GSK Clinical Trials
GlaxoSmithKline
Study Design
- Study Type
- observational
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 5, 2011
First Posted
May 30, 2011
Study Start
August 1, 2010
Primary Completion
January 1, 2011
Study Completion
January 1, 2011
Last Updated
December 1, 2016
Record last verified: 2016-11