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The Effect of Using Candesarsan and Amlodipine for Hypertensive Patients with Dyslipidemia in Japan

The Effect of Using Candesarsan and Amlodipine for Hypertensive Patients with Dyslipidemia in Japan - EARTH-trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000005817
Enrollment
40
Registered
2011-06-22
Start date
2011-07-01
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, Dyslipidemia

Interventions

None listed

Sponsors

The Cardiovascular Institute
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Hypertensive patients Systolic blood pressure>140 mmHg or Diastolic blood pressre.90 mmHg or Already taking antihypertensive drugs 2. High levels of LDL cholesterol patients LDL-C>140 mg/dl or LDL-C>100 mg/dl and need to take statints by attending physician or Already taking statins

Exclusion criteria

Exclusion criteria: 1.Malignancy 2.Contraindication to take candesartan, amlodipine and pitabastatin. 3.Familial hypercholesterolemia 4.Acute coronary syndrome 5.Already enrollment other clinical trials. 6.Mismatched patients

Design outcomes

Primary

MeasureTime frame
The blood pressure-lowering effect was not significant difference among candesartan and amlodipine groups. Moreover, candesartan group was not worsening insulin resistance and the effect of lipid metabolism in hypertensive patients with dyslipidemia.

Countries

Japan

Outcome results

None listed

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