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A multicenter study to examine renal protection by a combination of an HMG-CoA reductase inhibitor and losartan in patients with dyslipidemia associated with IgA nephropathy

A multicenter study to examine renal protection by a combination of an HMG-CoA reductase inhibitor and losartan in patients with dyslipidemia associated with IgA nephropathy - LIPS study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002887
Enrollment
80
Registered
2009-12-14
Start date
2009-12-01
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

IgA nephropathy

Interventions

statin and losartan group: simvastatin 5mg and Losartan 50mg/day more than 3 months statin group: simvastatin 5mg/day more than 3 months

Sponsors

Fukuoka University Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Men and women over the age of 20 2.Patients with dislipidemia(LDL cholesterol: 120 mg/dL or higher) 3.Patients who need a therapy of hypertention (JSH2009) 4.Patients not taking an ACE inhibitor or ARB within the last 3 months 5.Patients who have provided written consent

Exclusion criteria

Exclusion criteria: 1.Patients with type 1 diabetes mellitus 2.Patients with cardiovascular disease and with the following conditions Patients who have undergone coronary artery bypass grafting (CABG) or percutaneous transluminal coronary angioplasty (PTCA) within the last 3 months, patients with unstable angina, patients with a history of myocardial infarction, patients with a history of a transient ischemic attack (TIA) within the last 6 months, patients that are NYHA functional class III or IV or with heart failure, and patients with a history of cerebral infarction within the last 3 months 3. serum Cr>2.5mg/dL or eGFR<30mL/min 4.Patients with severe liver dysfunction 5.Patients with secondary hypertension caused by factors other than diabetes mellitus 6.HbA1c > 9% 7.Patients with pregnancy or nursing 8.Other patients deemed ineligible by an investigator

Design outcomes

Primary

MeasureTime frame
The effectiveness of reducing proteinuria in spot urine samples will be compared in a control group receiving statin therapy alone for 2 years and a treatment group given statin therapy and losartan.

Countries

Japan

Contacts

Public ContactSatoru Ogahara

Fukuoka University Faculty of Medicine Division of Nephrology and Rheumatology, Department of Internal Medicine

sogahara@cis.fukuoka-u.ac.jp+81-92-801-1011

Outcome results

None listed

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