MULTICENTER PROBE STUDY-4; COMPARISON OF THE EFFECTS OF ANGIOTENSIN II TYPE 1 RECEPTOR BLOCKERS
Not Applicable
- Conditions
- Hypertension
- Registration Number
- JPRN-UMIN000012768
- Lead Sponsor
- Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Department of Medicine and Clinical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Not provided
Exclusion Criteria
The patients with, 1)severe renal failure (sCr>2.0mg/dl), 2)severe hepatic dysfunction (AST/ALT>100IU/l), 3)the history of severe side effect of ARB 4)pregnancy or lactation, 5)malignancy or other poor-prognosis disease, 6)those who are considered inappropriate by physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in the clinic and home blood pressure
- Secondary Outcome Measures
Name Time Method renal function (Cr, eGFR, K), u-Alb/Cr, u-Na/Cr, lipid profile (LDL-C, HDL-C, T.Cho), others markers, and final dosage of the drug