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Clinical Trial Summary

The contribution of this study is the unedited evaluation of the circadian autonomic profiles of resistant hypertension with and without white-coat response.


Clinical Trial Description

All patients were submitted to office blood pressure measurement, Ambulatory blood pressure monitoring and 24-hour Holter monitoring.

Baseline blood samples for the measurement of glycemia (mg/dL), total cholesterol (mg/dL), LDL cholesterol (mg/dL), triglycerides (mg/dL), creatinine (mg/dL), serum uric acid, serum sodium, serum potassium, plasma aldosterone concentration (PAC) and plasma renin activity (PRA) were collected at 08:00 after overnight fasting. ;


Study Design

Observational Model: Cohort


Related Conditions & MeSH terms


NCT number NCT01833429
Study type Observational [Patient Registry]
Source University of Campinas, Brazil
Contact
Status Completed
Phase N/A
Start date September 2011
Completion date December 2012

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