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Examination of the effect of renal protection of aliskiren in chronic renal failure patient with hypertension (preservation period)

Examination of the effect of renal protection of aliskiren in chronic renal failure patient with hypertension (preservation period) - The Effect of Renal protection of Aliskiren in CRF with HT (preservation period) (ERA-CRF HT trial)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002478
Enrollment
200
Registered
2009-10-01
Start date
2009-11-01
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 renal failure patient with hypertension under going rennin-angiotensin treatment (ARB/ACE-inhibitor) (preservation period)

Interventions

Another antihypertensive agents (aliskiren is excluded) are oral-administrating or ARB/ACE inhibitor is increased in patients under the treatment of ARB/ACE inhibitor. If BP dose not reach to lower

Sponsors

Kure Kyousai Hospital
Lead Sponsor
Chuo Naika Clinic
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Fulfill all the following requirements at the time of the examination beginning. (1) Chronic renal failure patient with hypertension (preservation period), eGFR <60ml/min/1.73m2,and urinary protein is positive. (2) Patients under the treatment with ARB or ACE inhibitor (administrating for 6 months at the time of the examination beginnig at least.) (3)Patients who can acquire agreement with document when participating in research

Exclusion criteria

Exclusion criteria: Patient who much as one of the following items excludes from the examination object. (1)Active artery disease(within 6months of the clinical research beginning, patients who have unstable AP,MI,TIA,cerebrovascular disease,coronary bypass) (2)Patients administrating with Cyclosporin (3) Woman who has pregnant or possibility of pregnancy. (4) Patients who is important or unstable physically or mentally, and who is considerd to ruin a safety of patient and a participation to clinical research by the research doctor. (5)Additionally, patients who thought that doctor is improper.

Design outcomes

Primary

MeasureTime frame
(1)Comparison with urinary protein and serum Cr between aliskiren group and non-aliskiren group. (2)Comparison with urinary protein and serum Cr before and after administering aliskiren in aliskiren group.

Secondary

MeasureTime frame
(1)Office blood pressure(BP) (2)Estimated glomerular filtration rate(eGFR)calculated using the modified MDRD formula in the Japanese Society of Nephrology:eGFR(ml/min/1.73m2)=194 x age -0.287 x serum Cr -1.094(multiply by 0.739 in female) (3)CCr (4)Dialysis shift rate (5)Cardiovascular events (Stroke or transient ischaemic attack,New or recurrent acute myocardial infection,New occurrence or exacerbation of angina pectoris needing hospitalization,New occurrence or exacerbation of heart failure needing hospitalization,All-cause mortality)

Countries

Japan

Contacts

Public ContactTakao Masaki

Kure Kyousai Hospital Hiroshima University Hospital

masaki4221@gmail.com082-257-1506

Outcome results

None listed

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