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ARB+diurites vs ARB+Ca blocker

ARB+diurites vs ARB+Ca blocker - TAT Kobe

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005518
Enrollment
60
Registered
2011-04-27
Start date
2010-10-01
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

hypertension

Interventions

telmisaltan:40mg + HCTZ:12.5mg telmisaltan:40mg + amlodipine:12.5mg

Sponsors

Kobe University Hospital,Division of Cardiology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: hypertension patients who do not reach the target blood pressure with ARB only.

Exclusion criteria

Exclusion criteria: 1) uncontorable hypertension(DBP>110) 2) secondary hepertension 3) diabetes mellitus patient who are uncontorable(HbA1c>8.0%) or use insulin 4) stroke or myocardial infarction or severe cardiovascular disease within past 3 months 5) severe liver dysfunction 6) severe renal failure(Cr>2.0) 7) malignant disease 8) pregnancy woman 9) patient who can not secrete bille enoughly 10) hypersensivity for telmisaltan or HCTZ 11) hypersensivity for Tiazido type medicine 12) hypersensivity for Ca-blocker 13) patient who are judged inappropriate condition for study by doctor

Design outcomes

Primary

MeasureTime frame
blood pressure after 12 weeks

Secondary

MeasureTime frame
laboratory data:WBC,RBC,Hb,Hct,Plt,LDL-C,TG,HDL-C,AST,ALT,LDH,ALP,ganma-GTP,CK,FBS,IRI,Alb,BUN,Cr,UA,Na,K,Cl,PRA,aldsterone,U-Na,U-Cl,U-Cr,U-ALb,hs-CRP,HbA1c

Countries

Japan

Contacts

Public ContactTatsuro Ishida

Kobe University Hospital Cardiology

ishida@med.kobe-u.ac.jp078-382-5846

Outcome results

None listed

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