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Clinical Trials/JPRN-UMIN000003684
JPRN-UMIN000003684
Completed
未知

A comparison of twenty-four-hour blood pressure control between candesartan and other ARBs estimated by the ambulatory blood pressure monitoring - Effect of candesartan on 24-hours blood pressure control

Department of Integrated Medicine, Ehime University Graduate Schoolof Medicine0 sites50 target enrollmentJune 19, 2010

Overview

Phase
未知
Intervention
Not specified
Conditions
essential hypertension
Sponsor
Department of Integrated Medicine, Ehime University Graduate Schoolof Medicine
Enrollment
50
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 19, 2010
End Date
March 31, 2012
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Department of Integrated Medicine, Ehime University Graduate Schoolof Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. secondary hypertension 2\. systolic blood pressure \>160 mmHg and or diastolic blood pressure \> 100 mmHg 3\. malignant hypertension 4\. history of stroke, myocardial infarction and other cardiovascular disease that needed hospitalization within recent 6 months. 5\. atrial fibrillation 6\. patients with fundal hemorrhage, exudation or papilledema due to hypertensive retinopathy 7\. liver dysfunction(the levels of AST or ALT reached 250% of their upper normal limit.) 8\. Renal dysfunction (serum creatinine \> 2\.0 mg/dl) 9\. hyperkalemia (serum K \> 5\.5 mEq/l) 10\. pregnant or nursing women 11\. patients who are not recommended for participation in this study by physician in charge with medical reasons.

Outcomes

Primary Outcomes

Not specified

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