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Randomized, closs-over study to compare the effect of cilnidipine and azelnidipine on microalbuminuria in patients with hypertension and chronic kidney disease

Randomized, closs-over study to compare the effect of cilnidipine and azelnidipine on microalbuminuria in patients with hypertension and chronic kidney disease - Randomized, closs-over study to compare the effect of cilnidipine and azelnidipine on microalbuminuria in patients with hypertension and chronic kidney disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008553
Enrollment
40
Registered
2012-07-30
Start date
2012-07-30
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

hypertensive patients with chronic kidney disease

Interventions

cilnidipine(initial dose is 10mg/day, 5-20mg/day) azelnidipine(initial dose is 8mg/day, 4-16mg/day)

Sponsors

Department of Cardiology and Nephrology, Mie University, Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Hypertension patients with chronic kidney disease (CKD) *Chronic kidney disease is defined as either kidney damage or GFR<60ml/min/1.73m^2 for 3months. Kidney damage is defined as pathologic abnormalities or markers of damage, including abnormalities in blood or urine tests or imaging studies. Patients who administer angiotensin receptor blocker(ARB) and amlodipine as calcium blocker.

Exclusion criteria

Exclusion criteria: 1) Contraindication to calcium chanel blockers. 2) Patients who has already administered calcium channel blocker except for amlodipine. 3) Any serious comobidity(brain disease, heart disease, renal disease, hepatic disease) 4) The patients with pregnant or possibly pregnant 5) Sereous hypertension patients 6) Investigator judged as inappropriate for this study.

Design outcomes

Primary

MeasureTime frame
Urinary albumin-creatinie ratio(mg/g*Cr) after 12 and 24 weeks

Secondary

MeasureTime frame
Clinical blood pressure and heart rate Mean home blood pressure Estimated glomerular filtration rate Plasma Renin Activity, Plasma Aldosterone Concentration Antihypertensive effect Safety parameters will be analized after 12 and 24 weeks

Countries

Japan

Contacts

Public ContactMasaya Taniguchi

Mie University, Graduate School of Medicine Department of Cardiology and Nephrology

(059)231-5015

Outcome results

None listed

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