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ESES-LVH study

Efficacy and Safety of Esaxerenone in Hypertensive Patients with Left Ventricular Hypertrophy - ESES-LVH study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs071190043
Enrollment
120
Registered
2020-01-24
Start date
2020-06-26
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 Left Ventricular Hypertrophy Hypertensive Patients with Left Ventricular Hypertrophy

Interventions

The duration of treatment with Esaxelenone is 24 weeks. Esaxelenone is given orally once daily. The initial daily doses will be started at 2.5 mg and titrated (if the effect is insufficient, the dose

Sponsors

Tsujita Kenichi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients with hypertension (early morning home blood pressure [BP]: =>135 mmHg and 85 mmHg and <=99 mmHg of diastolic blood pressure) 2)Patients with left ventricular hypertrophy. 3)Patients treated with renin-angiotensin inhibitor or Ca-antagonist. 4)Patients aged 20 years or older.

Exclusion criteria

Exclusion criteria: 1)Patients with a diagnosis of secondary hypertension or malignant hypertension. 2)Patients with orthostatic hypotension or a history of orthostatic hypotension. 3)Patients with any of the cerebro-cardiovascular diseases. 4)Patients with type 1 diabetes. 5)Hyperkalemia patients, patients whose serum potassium level exceeds 5.0 mEq/L, etc. 6)Patients who the investigator judges to be unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
1)Change in sitting BP (early morning home BP) between baseline values and values at the end of administration of Esaxerenone. 2)Amount and rate of change in left ventricular mass index (LVMI) between baseline values and values at the end of administration of Esaxerenone.

Secondary

MeasureTime frame
1)Change in sitting BP (early morning home BP) between baseline and 12 weeks after the start of Esaxerenone administration. 2)Change in sitting BP (home BP before bedtime) between baseline values and values at the end of administration of Esaxerenone. 3)Proportion of patients achieving the target of sitting BP reduction. 4)Left Ventricular Mass (LVM) and Rate of change in left ventricular mass index (LVMI) between baseline and 12 weeks after the start of Esaxerenone administration. 5)Change in Left Ventricular posterior Wall Thickness (LVPWT), Relative Wall Thickness (RWT), the ratio between the E-wave velocity and A-wave velocity of the pulsed-wave Doppler mitral flow image (E/A), the ratio between E-wave velocity and the average early diastolic velocity of the lateral and septum at the mitral annulus level (E/e'), E-wave height, mitral annulus early diastolic velocity (e'), a', tricuspid regurgitation velocity (TRV), left atrial volume index (LAVI), left ventricular end-diastolic dimension (LVDd), deceleration time (DT), left ventricular ejection fraction (LVEF), vascular function test (baPWV or CAVI), myocardial strain, myocardial strain rate, left ventricular volume, left atrial volume,double product (DP), triple-product (TP), coefficient of variation of R-R Interval (CVR-R), NT-proBNP, CRP, PAC, PRA, and urinary (Na, K, albumin, creatinine, protein) between baseline and 12 weeks after the start of Esaxerenone administration.

Contacts

Public ContactDaisuke Sueta

Kumamoto University Hospital

Sueta-d@kumamoto-u.ac.jp+81-96-373-5175

Outcome results

None listed

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