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Evaluation of the efficacy of atorvastatin in patients with CKD

Evaluation of the efficacy of atorvastatin in patients with CKD - The efficacy of atorvastatin for CKD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009393
Enrollment
50
Registered
2013-01-07
Start date
2013-01-07
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CKD patients

Interventions

The patients with CKD accompanied by hyperlipidemia (n=50) were administered 10mg of atorvastatin orally once a day. However, the maximum daily dose of atorvastatin is 40mg. The period of this study i

Sponsors

Division of Nephrology, Juntendo University Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients are eligible if they are compatible with the following criteria. 1. CKD patients accompanied with hyperlipidemia. (administration of statin and /or ethyl icosapentate are not restricted) 2. Patients who agreed with the participation of the study based on informed consent before the study initiation, and filled in signature sealing or a signature and a date.

Exclusion criteria

Exclusion criteria: Patients are excluded if they are compatible with any one of the following criteria. 1. Patients with a history of hypersensitivity for an ingredient of atorvastatin. 2. Patients whose liver function is thought to decrease; acute hepatitis, acute aggravation of the chronic hepatitis, cirrhosis, liver cancer, jaundice 3. A pregnant woman or the woman who may be pregnant and nursing mother. 4. Patients receiving telaprevir. 5. Patients with significant psychic disturbance or drug dependence disease or alcoholism. 6. Patients that going to hospital of all follow-up seems to be impossible. 7. Patients who are not able to understand a test instruction from medical experts of the client side or the doctors involved in the study. 8. Patients who judged as inadequate by the doctors involved in the study.

Design outcomes

Primary

MeasureTime frame
Amount of urinary albumin

Secondary

MeasureTime frame
1.Lipid metabolism: LDL, HDL, TG, Apolipoprotein fractionation, MDA-LDL 2.High sensitive CRP 3.ADMA 4.Urinary L-FABP 5.Urinary 8-OHdG 6.ABI and CAVI 7.Carotid ultrasonography 8.Examination of the fundus

Countries

Japan

Contacts

Public ContactHitoshi Suzuki

Juntendo University Faculty of Medicine Department of Internal Medicine, Division of Nephrology

shitoshi@juntendo.ac.jp03-5802-1065

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026