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Effects of eplerenone on glucose metabolism and blood pressure in hypertensive patients with obesity

Effects of eplerenone on glucose metabolism and blood pressure in hypertensive patients with obesity - Kurume Eplerenone Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009127
Enrollment
200
Registered
2012-11-01
Start date
2012-11-01
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

Eplerenone (Trade name: Selara, Pfizer Inc.)50mg once a day Trichlormethiazide (Trade name: Fluitran, Shionogi &amp
Co., Ltd.)1mg once a day

Sponsors

Departmenet of Internal Medicine Division of Cardio-Vascular Medicine and Department of Community Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Out Patients 2.Patients who are with BMI >=25kg/m2 and SBP>=140mmHg and/or DBP>= 90mmHg at consalting room

Exclusion criteria

Exclusion criteria: 1.Patients on eplerenone or spironolactone during 3 months prior to enrollment 2.Patients on diuretics including trichlormethiazide or combination drugs during 3 months prior to enrollment 3. Patients who experienced myocardial infarction or stroke during 30 days prior to enrollment 4.Patients who had cardiac surgery or PCI during 30 days prior to enrollment 5. Patients with serum potassium >= 5.0 mEq/L 6.Patients with severe liver dysfunction 7.Patients with severe renal dysfunction 8.Patients with grade III hypertension (SBP >=180mmHg and/or DBP >=110mmHg) 9.Patients diagnosed as having secondary hypertension 10.Patients with hypersensitivity with eplerenone or sulfonamide derivative 11.Patients who are contraindicated for use of eplerenone or trichlormethiazide 12.Patients who are on medications contraindicated for use with eplerenone or trichlormethiazide 13.Women who are either pregnant, lactating or of childbearing potential 14.Patients who are considered not appropriate to enroll into this trial under the judgment of the investigator

Design outcomes

Primary

MeasureTime frame
Change from baseline in office SBP/DBP after 24 weeks Change from baseline in insulin sensitivity (homeostasis model assessment insulin resistance (HOMA-IR)) after 24 weeks Change from baseline in HbA1c after 24 weeks

Secondary

MeasureTime frame
Changes from baseline in hsCRP, eGFR, and adiponectin

Countries

Japan

Contacts

Public ContactHisashi Adachi

Kurume University School of Medicine Departmenet of Internal Medicine Division of Cardio-Vascular Medicine and Department of Community Me

hadac@med.kurume-u.ac.jp+81-942-31-7586

Outcome results

None listed

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