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Therapeutic effects of direct renin inhibitor aliskiren added to AT1 receptor blocker in hypertensive patients with chronic kidney disease.

Therapeutic effects of direct renin inhibitor aliskiren added to AT1 receptor blocker in hypertensive patients with chronic kidney disease. - Therapeutic effects of direct renin inhibitor aliskiren added to AT1 receptor blocker in hypertensive patients with chronic kidney disease.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002546
Enrollment
100
Registered
2009-09-25
Start date
2009-09-01
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

Hypertension Chronic kidney disease

Interventions

ACE inhibitor group: Patients are initially given 2.5 mg of benazepril once daily for 24 weeks. The dosse of benazepril can be titrated up to 10 mg daily as needed. Direct renin inhibitor group: Patie

Sponsors

Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Hypertensive patients with chronic kidney disease who are already receiving standard doses of AT1 receptor blocker but without achievement of blood pressure lowering to target blood pressure levels.

Exclusion criteria

Exclusion criteria: 1. Dialysis patients 2. Patients with history of angioedema 3. Patients on apheresis therapy 4. Patients taking cyclosporin 5. History of hypersensitivity to benazepril and/or aliskiren 6. Pregnant women and/or women who are suspect of pregnancy 7. Patients judged as inappropriate for the study

Design outcomes

Primary

MeasureTime frame
1. Blood pressure (clinical BP, ABPM) 2. Renal function (s-Cr, eGFR, urinary protein/albumin excretion)

Secondary

MeasureTime frame
1. Glucose metabolism (FBS, HbA1C, IRI, HOMA-IR) 2. Lipid metabolism (TCHO, LDLC, HDLC, TG) 3. Sympathetic nerve activity, renin-angiotensin system (PRA, PAC, catecholamine, urinary AGT) 4. Oxidative stress (urinary L-FABP, serum pentosidine) 5. Cardiovascular function (BNP, UCG, PWV, central blood pressure) 6. Adverse events

Countries

Japan

Contacts

Public ContactKouichi TAMURA

Yokohama City University School of Medicine Department of Cardiorenal Medicine

tamukou@med.yokohama-cu.ac.jp045-787-2635

Outcome results

None listed

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