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To Study the effect of Empagliflozin on the cardiovascular biomarkers in diabetic patients myocardial infarction

To Study the effect of Empagliflozin on the cardiovascular biomarkers Galectin-3 and sST-2 in type 2 diabetic patients myocardial infarction with requiring primary angioplasty

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230724058910N1
Enrollment
60
Registered
2023-08-07
Start date
2023-08-23
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Condition 1: Myocardial Infarction. Condition 2: Type 2 diabetes. Acute transmural myocardial infarction of unspecified site Type 2 diabetes mellitus without complications

Interventions

Intervention 1: Intervention group: In this group, 30 type 2 diabetic patients treated with oral drugs, and they will receive empagliflozin from ABIDI Pharmaceutical Company in the form of 10 mg table

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor
Abidi Pharmaceutical Company
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Type 2 diabetic patients (Hb A1C: 6.5-8) Diabetes treated with oral agents Typical chest pain during the 12 hours before presentation lasting more than 30 minutes ST- segment elevation above 0.1 mV in two leads or more in ECG

Exclusion criteria

Exclusion criteria: Cardiogenic shock Diabetic ketoacidosis History of CABG Type 1 diabetic patients Severe liver failure End stages cancer or history of any cancer History of severe allergy to empagliflozin or its formulation components Severe renal failure (eGFR <30 mL/minute/1.73 m2), end-stage renal disease (ESRD), or dialysis Hypovolemia Any inflammatory disease under treatment Advanced heart failure Hypoglycemia

Design outcomes

Primary

MeasureTime frame
Galectin-3 gene expression. Timepoint: Measurement of Galectin-3 gene expression at the beginning of the study (before intervention) and 3 months after starting empagliflozin. Method of measurement: RT-PCR.;SST2 gene expression. Timepoint: Measurement of sST2 gene expression at the beginning of the study (before intervention) and 3 months after starting empagliflozin. Method of measurement: RT-PCR.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Yousefi Ramandi

Zanjan University of Medical Sciences

mahnaz.yousefi@gmail.com+98 912 883 3831

Outcome results

None listed

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