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Second choice of antihypertensive drugs for lowering of proteinuria effective combination therapy in CKD trial

Second choice of antihypertensive drugs for lowering of proteinuria effective combination therapy in CKD trial - Second choice of antihypertensive drugs for lowering of proteinuria effective combination therapy in CKD trial(SELECT-CKD TRIAL)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003455
Enrollment
100
Registered
2010-04-06
Start date
2010-04-01
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

Hypertensive patients with CKD under the treatment of ARB

Interventions

ACE-inhibitor is added on pretreatment(ARB) Cilnidipine is added on pretreatment(ARB)

Sponsors

Tokyo Women's Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Hypertensive patients with CKD fulfilled following conditions during observation period will be enrolled (targeted) 1. SBP>=130mmHg or DBP>=80mmHg 2. Treated by ARB more than 1 month, and not treated by CCB or ACE inhibitor last 1 month 3. Written informed consent for this study is obtained 4. Obvious Renal damage 1) Proteinuria, pathology diagnostic imaging, urine or blood tests etc. 2) GFR=<60mL/min/1.73m2

Exclusion criteria

Exclusion criteria: Following patients will be excluded from this study 1.Hypertensive emergency that requires other than oral administration of antihypertensives 2.Past history of severe adverse effect by CCB, ARB, or ACE inhibitor 3.Cerebrovascular disease occured within 6 months 4.Severe liver or renal dysfunction 5.Sever heart failure (NYHA class >= 3), severe arrhythmia (frequent ventricular or atrial extrasystole, sustained ventricular tachycardia, atrial arrhythmia with severe tachycardia, atrial fibrillation or flutter with severe bradycardia, sick sinus syndrome with severe bradycardia, atrio-ventricular block with severe bradycardia), myocardial infarction within 6 months 6. Malignancy 7. Pregnant, possible to be pregnant, or willing to be pregnant 8. Scheduling the operation 9. Patients who are inadequate by physician's decision

Design outcomes

Secondary

MeasureTime frame
1 Change in CKD stage 2 Serum Cr 3 Estimated GFR 4 Serum beta2-microglobulin 5 Urinary L-FABP 6 Serum CRP 7 Plasma BNP 8 Echocardiography 9 ICG 10 PAI-1 11 Serum ADMA 12 Serum uric acid 13 Cardiovascular events Cerebrovascular and cardiovascular mortality fatal myocardial infarction, fatal heart failure, sudden death, fatal stroke, other cardiovascular death Hospitalization due to cerebrovascular and cardiovascular disease nonfatal myocardial infarction, angina, heart failure, cerebral bleeding, cerebral infarction, transient cerebral ishemic attack 14 Blood pressure lowering effect 15 Heart rate 16 Safety

Primary

MeasureTime frame
1. Change in urinary protein 2. Change in baPWV

Countries

Japan

Contacts

Public ContactTetsuya Ogawa

Tokyo Women's Medical University Department of Medicine, Kidney Center

03-3353-8111

Outcome results

None listed

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