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Renoprotective Effect of ALiskiren in Japanese Hypertensive Patients

Renoprotective Effect of ALiskiren in Japanese Hypertensive Patients - Kanazawa REAL trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005441
Enrollment
200
Registered
2011-04-15
Start date
2011-04-01
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

Interventions

A standard dose ARB+Aliskiren 150mg/day A high dose ABR monotherapy

Sponsors

Kanazawa Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Hypertensive patients who are older than 30 years. (2) Hypertensive patients whose blood pressure cannot achieve less than 140/90 mmHg under treatment with a standard dose of ARB over 4 weeks. (3) Outpatients who give written informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients who have secondary hypertension (2) Patients with serum Cr =>2.0 mg/dL (3) Patients who have previous history of allergy to Aliskiren (4) Patients who are pregnant or have possibility of pregnancy and are lactation period (5) Patients who have ciclosporin or itraconazole (6) Patients who have bilateral or unilateral renal artery stenosis (7) Patients who have hyperkalemia (8) Patients who have nephrotic syndrome (9) Patients who were deemed not appropriate to participate in this study by doctor

Design outcomes

Primary

MeasureTime frame
(1) Change in blood pressure (2) Change in albuminuria

Secondary

MeasureTime frame
Change before and after treatment of the following items: (1) PRA, PAC, serum creatinine, potassium (2) Change in eGFR

Countries

Japan

Contacts

Public ContactHiroshi Takakuwa

Kanazawa Municipal Hospital Department of Internal Medicine

Outcome results

None listed

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