Effect of azilsartan on 24-h ambulatory blood pressure in patients with CKD and hypertension.
Not Applicable
- Conditions
- CKD and hypertension
- Registration Number
- JPRN-UMIN000012931
- Lead Sponsor
- ephrology and Hypertension, St. Marianna University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion criteria were known hypersensitivity to ARBs, ACE inhibitors or direct renin inhibitors and pregnancy or lactation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint was 24-h systolic BP by ambulatory monitoring.
- Secondary Outcome Measures
Name Time Method