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Comparison of effects of aliskiren-based combination therapy between CCB and ARB in hypertensive patients with chronic kidney disease

Comparison of effects of aliskiren-based combination therapy between CCB and ARB in hypertensive patients with chronic kidney disease - Comparison of effects of aliskiren-based combination therapy between CCB and ARB in hypertensive patients with chronic kidney disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006821
Enrollment
100
Registered
2011-12-02
Start date
2011-12-01
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

Hypertension, chronic kidney disease

Interventions

CCB group: In the intervention phase, add-on combination therapy will be performed by amlodipine 2.5-10 mg daily for 24 weeks. ARB group: In the intervention phase, add-on combination therapy will b

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: 1) Chronic kidney disease.3) 2) On monotherapy by aliskiren 150 mg daily. 3) Clinic SBP >= 130 mmHg or clinic DBP>=80 mmHg.

Exclusion criteria

Exclusion criteria: 1) CKD stage 5 or on dialysis therapy 2) History of hypersensitivity to aliskiren, amlodipine, or valsartan. 3) Pregnant or suspicious women. 4) Treatment with itraconazole, cyclosporine. 5) Judged as inappropriate for the study

Design outcomes

Primary

MeasureTime frame
1.Body weight, BMI, abdominal circumference. 2.Clinic BP 3.Home BP 4.Ambulatory BP 5.Renal function (eGFR), urinary protein and albumin excretion, urinary sodium excretion. Urinary type IV collagen and angiotensinogen. 6.Vascular function. Central BP, ABI/PWV, FMD. 7.Glucose metabolism markers. 8.Lipid metabolism markers. 9.Endocrine system. PRA, PAC, BNP. 10.Inflammatory and oxidative stress markers.

Countries

Japan

Contacts

Public ContactKouichi Tamura

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

tamukou@med.yokohama-cu.ac.jp045-787-26358

Outcome results

None listed

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