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Comparison of the effect of sprinolactone with eplerenone on metabolic profile in patients with reduced left ventricular function

Investigating the effect of spironolacton compared to eplerenon on the metabolic profile and left ventricular function in patients with heart failure reduced EF referred to Rasoul Akram Hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240823062849N1
Enrollment
50
Registered
2024-12-25
Start date
2024-05-15
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: HEART FAILURE. Condition 2: DIABETES. Heart failure Diabetes mellitus due to underlying condition

Interventions

Intervention 1: Intervention group:Spironolactone tablets, 25 mg daily, are prescribed to the patient after daily tests are taken. Then, after 1 week, if tolerated and the tests are normal, the dose i

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: over age of 18 years EF < 50% Patients with diabetes on oral medication or pre diabetes Not using mineralocorticoid antagonist drugs

Exclusion criteria

Exclusion criteria: Age less than 18 years old paitents with chronic lung, liver and kidney diseases at the same time pregnancy Taking insulin at the same time History of complications with sprinolactone or eplerenone Cr > 2 the patient is not able to take medicines orally

Design outcomes

Primary

MeasureTime frame
Hemoglobin A1C. Timepoint: intial - after 4 month. Method of measurement: A venous blood sample was taken from the patient by a laboratory technician at Rasoul Akram Hospital.;Fasting Blood Suger. Timepoint: intial - after 4 month after startig use of the drug. Method of measurement: A venous blood sample was taken from the patient by a laboratory technician at Rasoul Akram Hospital.;Left ventricular ejection function. Timepoint: intial - after 4 month after startig use of the drug. Method of measurement: Echocardiography.;Brain natriuretic peptide. Timepoint: intial - after 4 month after startig use of the drug. Method of measurement: A venous blood sample was taken from the patient by a laboratory technician at Rasoul Akram Hospital.

Secondary

MeasureTime frame
Complete blood count. Timepoint: intial - After 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Blood Urea Nitrogen. Timepoint: intial- after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Creatinin. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Sodium. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Potassium. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Triglyceride. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Low density lipoprotein. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;High density lipoprotein. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Cholestrol. Timepoint: intial - after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.;Troponin. Timepoint: initial -after 4 month starting the use of drug. Method of measurement: A venous sample was taken from the patient by a laboratory technician.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh vahmani

Iran University of Medical Sciences

Fatemehvahmani@yahoo.com009864350000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026