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The effect of empagliflozin laboratory findings

Assessment the effects of Empagliflozin on laboratory markers in type 2 diabetic patients with coronary artery disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190412043247N1
Enrollment
100
Registered
2019-10-05
Start date
2019-05-21
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Condition 1: Diabetes Mellitus type 2. Condition 2: Coronary artery disease. Type 2 diabetes mellitus Atherosclerotic heart disease of native coronary artery

Interventions

Intervention 1: Intervention group: The 50 patients in the intervention group will be treated with Empagliflozine 10 mg daily for 6 months (made by Abidi Pharmaceutical Company). Intervention 2: Contr

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age between 40-75 year-old HbA1c between 6.5 to 9 Diabetes mellitus type 2 Under fix continues treatment for at least 3 month BMI less than 40 Fixed Diet and physical activity

Exclusion criteria

Exclusion criteria: Pregnancy Heart Failure (NYHA class 3-4) History of allergic reaction to SGLT2 inhibitors Drugs History of SGLT2 inhibitor Drugs usage GFR3 times upper normal limit Presence of urinary-genital infection History of infection less than 1 month prior to the study History of Anti-inflammatory drugs

Design outcomes

Primary

MeasureTime frame
Changes hs-Troponin-I. Timepoint: At the begining of the study, befor the intervention and 6 month after the intervention. Method of measurement: Laboratory Measurments.;Changes in level of hs-CRP. Timepoint: At the begining of the study, befor the intervention and 6 month after the intervention. Method of measurement: Laboratory Measurments.;Changes in level of lipid profile. Timepoint: At the begining of the study, befor the intervention and 6 month after the intervention. Method of measurement: Laboratory Measurments.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHoma Taheri

Zanjan University of Medical Sciences

homataheri88@gmail.com+98 24 3313 0001

Outcome results

None listed

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