Prospective evaluation of renal function and proteinuria in chronic kidney disease patients
Not Applicable
- Conditions
- Proteinuria
- Registration Number
- JPRN-UMIN000007371
- Lead Sponsor
- Aichi welfare agricultural cooperative association Anjo Kosei Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
The patient who caused acute coronary syndrome within six months. The patient of an inflammatory disorder, infection, and a malignant tumor. The patient who has an anamnesis of hypersensitivity to atorvastatin and/or rosuvastatin. A pregnant woman or the woman that may have become pregnant, and a nursing mother. A patient with critical impaired liver function and renal dysfunction.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change of the protein in urine / creatinine ratio after 52 weeks
- Secondary Outcome Measures
Name Time Method Change of the protein in urine / creatinine ratio after 26 weeks Change of the albumin in urine / creatinine ratio after 26 weeks and 52 weeks Lipid rate of change after 26 weeks and 52 weeks Change of eGFR after 26 weeks and 52 weeks