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Effect of Losartan/HCTZ on diastolic function in patients with hypertension 2 Comparison with ARB/CCB combined therapy

Effect of Losartan/HCTZ on diastolic function in patients with hypertension 2 Comparison with ARB/CCB combined therapy - Effect of ARB/Diuretics on left ventricular diastolic dysfunction EDEN 2

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004080
Enrollment
400
Registered
2010-09-01
Start date
2010-07-01
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 patients with left ventricular diastolic dysfunction

Interventions

ARB/HCTZ ARB/CCB

Sponsors

Diastolic Dysfunction Study Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Hypertension patients are those who have been treated with anti hypertensive therapy including ARB usual dose and whose blood pressure has not been sufficinetly controlled Left ventricular diastolic dysfunction patients LVEF >=50% e'<8cm/s and or E/e' >=15 Outpatiens Obtaining written informed consent

Exclusion criteria

Exclusion criteria: Insufficiently controlled hypertension DBP more than 110mmHg Secondary hypertension Diabetes mellitus patient under insulin treatment Onset of myocardial infarction or stroke within 6 months before recruiting Concurrent hepatic dysfunction GPT more than 3 times the upper limit of normal values Renal dysfunction sCr more than 2.0 mg/dL Gout or hyperuricemia uric acid more than 8.0 mg/dL Heart failure with NYHA 3 or more AF undergo echocardiography Valvular disease Malignant tumor and/or poor prognosis severe disease Women who are pregnant, enable to be pregnant, or are breastfeeding Concurrent treatment with diuretics and/or CCB Hypersensitivity or allergy to losartan, HCTZ and amlodipine Hypersensitivity or allergy to thiazide and other analogs Patients who are determined by the investigators to be unsuitable

Design outcomes

Primary

MeasureTime frame
Change in e' and e'/E

Countries

Japan

Outcome results

None listed

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