Hypertention
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with hypertention who have not attained the target blood pressure level established by the Japan Society of hypertention 2009 guidelines. 2. Patients giving written consent on their own volition for participation in this clinical trial after being provided with sufficient explanation about the study.
Exclusion criteria
Exclusion criteria: 1. Patients who have a contraindication to Selara TAB administration. 2. Patients who have a contraindication to Norvasc TAB administration . 3. Patients with liver dysfunction (AST or ALT values of >=100IU). 4. Patients who are judged by the investigator to be not eligible for enrollment in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in atrial late potentials recorded by P wave signal-averaged ECG. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Correlation between baseline characteristics and atrial late potentials. 2. Correlation between change in atrial late potentials and change in blood biomarkers. | — |
Countries
Japan
Contacts
Osaka General Medical Center Division of Cardiology