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Clinical Trials/JPRN-C000000280
JPRN-C000000280
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Study for the effectiveness of intensive therapy for diabetic nephropathy in unblinded, randomized intergroup comparison study. - Study for the effectiveness of intensive therapy aiming at a remission of diabetic nephropathy (DNETT-Japan)

Okayama University Hospital0 sites600 target enrollmentNovember 16, 2005

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Okayama University Hospital
Enrollment
600
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 16, 2005
End Date
June 1, 2011
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Patients who fall into the following categories are not eligible:1\) Patients with type 1 diabetes mellitus2\) Patients with hereditary diabetes mellitus or secondary diabetes mellitus.3\) Patients with non\-diabetic nephropathy, e.g., glomerular nephritis, lupus nephritis.4\) Patients with familial hypercholesterolemia.5\) Patients with secondary hypertension.6\) Patients with unstable angina pectoris, or patients who have developed myocardial infarction or cerebral hemorrhage within 6 months prior to the observation period.7\) Patients with any life\-threatening disease which will be the cause of death within five years such as malignant tumor.8\) Patients with a history of angio edema.9\) Patients under LDL\-apheresis by a adsorber with dextran sulphate cellose.10\) Patients with biliary obstruction or severe hepatopathy.11\) Patients considered as having hypergasia of hepatic metabolism such as acute hepatitis, acute exacerbation of chronic hepatitis, cirrhosis, hepatic cancer, or jaundice.12\) Patients with a history of hypersensitivity against ACE inhibitors, ARBs, or HMG\-CoA reductase inhibitors.13\) 0patiens, and patients who want to become pregnant during the study period.14\) Other patients judged as being inappropriate for the subjects of the study by investigators.

Outcomes

Primary Outcomes

Not specified

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