This phase II study examines the safety and efficacy of combination therapy for hypertension in patients with autosomal dominant polycystic kidney disease (ADPKD). This study examines the safety and efficacy of combination therapy by imidapril (ACEI) or cilnidipine (CCB) in ADPKD patients whose blood pressure is not controlled under 120/80 mmHg by candesartan (ARB) alone.
Maximum dosage of candesartan is 8 mg/day. Dosage of imidapril is in the range of 2.5-10 mg/day. Dosage of cilnidipine is in the range of 5-20mg/day.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
160
Cilnidipine up to 20 mg
Imidapril up to 10 mg per day
Department of Urology, National Hospital Organaization Chiba-East Hospital
Chiba, Chiba, Japan
NOT_YET_RECRUITINGDepartment of Medicine II, Hokkaido Univserity School of Medicine
Sapporo, Hokkaido, Japan
RECRUITINGeGFR
Time frame: every 6 months
Kidney Volume measured by MRI
Time frame: every 3 months to every 2 years
Serum creatinine level
Time frame: every 3 months to every 2 years
Induction of hemodialysis, cardiovascular events and central nervous vascular events
Time frame: every 3 months to every 2 years
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Toranomon Hospital Kajigaya, Kidney center
Kawasaki, Kanagawa, Japan
NOT_YET_RECRUITINGDivision of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences
Niigata, Niigata, Japan
NOT_YET_RECRUITINGDepartment of Medicine II, Nippon Medical School
Bunkyo-ku, Tokyo, Japan
NOT_YET_RECRUITINGDepartment of Urology, Teikyo University School of Medicine
Itabashi-ku, Tokyo, Japan
RECRUITINGToranomon Hospital, Kidney center
Minato-ku, Tokyo, Japan
NOT_YET_RECRUITINGDivision of Kidney and Hypertension, Department of Internal Medicine, Jikei University School of Medicine
Minato-ku, Tokyo, Japan
ACTIVE_NOT_RECRUITINGDepartment of Urology, Kyorin University School of Medicine
Mitaka, Tokyo, Japan
NOT_YET_RECRUITING