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Effect of direct renin inhibitor(Aliskiren) in chronic heart failure patient with hypertension

Effect of direct renin inhibitor(Aliskiren) in chronic heart failure patient with hypertension - Effect of direct renin inhibitor(Aliskiren) in chronic heart failure patient with hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005719
Enrollment
100
Registered
2011-06-04
Start date
2011-06-01
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

chronic heart failure

Interventions

Observing during one year after changing to aliskiren 150mg/day from ARB

Sponsors

Anjo Kosei Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patient who is in stable control at registration 2)Patient who is not taking aliskiren within one month before registration 3)Patient who is taking ARB of standard dosage 4)Patient who obtained agreement by free will of patient himself on full understanding after enough explanation

Exclusion criteria

Exclusion criteria: 1)Patient who has hypersensitivity and the past in direct renin inhibitor 2)Patient treated by ACE inhibitor 3)Patient with poor control of diabetic mellitus(HbA1c 9% or more) 4)Patient with unstable angina pectoris or who has the past history of acute myocardial infarction and cerebral infarction within three months 5)Patient with LVEF<30% 6)Patient who has serious liver disease (child classification C or more) 7)Patient who has serious kidney disease 8)Patient who is taking medicine of contraindication of using together 9)Woman who has possibility of pregnancy or getting pregnant 10)Breast-feeding woman 11)Patient with hyperkalemia(5.5mEq/L or more) 12)Patient of eGFR<30mL/min/1.73 m2 13)Additionally, patient who judged to be improper as testee

Design outcomes

Primary

MeasureTime frame
Changes in serum brain natriuretic peptide level

Secondary

MeasureTime frame
Changes in LVEF,blood pressure,PRA,plasma aldosterone level,serum potassium level,eGFR,serum creatinine level,albuminuria,uric acid level

Countries

Japan

Contacts

Public ContactTadahiro Ito

Anjo Kosei Hospital Division of Cardiovascular Medicine

semiyontd17@gmail.com0566-75-2111

Outcome results

None listed

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