Blood sampling
OtherBlood sampling for Fasting Plasma Glucose, Hemoglobin A1C, Cholesterols, Blood Urea Nitrogen, Creatinine
Other names: Blood sampling for cardiovascular disease risk
NCT Number: NCT01362283
The purpose of this study is investigating the proportion of Cardiovascular disease risk factors of hypertensive patients.
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Notify Me18 year and older
All sexes
Observational
Primary endpoint: To evaluate the Proportion of patients with Cardiovascular disease high risk factors
Secondary endpoint: To evaluate the Proportion of patients with Cardiovascular disease risk factors, To evaluate the Proportion of patients with Cardiovascular disease, To evaluate Target blood pressure achievement rate according to the proportion of Cardiovascular disease risks
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Blood sampling for Fasting Plasma Glucose, Hemoglobin A1C, Cholesterols, Blood Urea Nitrogen, Creatinine
Other names: Blood sampling for cardiovascular disease risk
Time frame: 6years, average duration of hypertension
Between patients with essential hypertension
Time frame: 6years, average duration of hypertension
Between patients with essential hypertension
Time frame: 6years, average duration of hypertension
Between patients with essential hypertension
Time frame: 6years, average duration of hypertension
Between patients with essential hypertension
GlaxoSmithKline
Industry
A Multi-center, Observational, Cross-sectional Study to Evaluate CVD Risk Factors in Korean Hypertensive Patients
Acronym: WONDeR
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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