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A single-center, prospective, double-blind, randomized controlled trial of dapagliflozin in improving ventricular remodeling in patients with left ventricular dysfunction after acute myocardial infarction

A single-center, prospective, double-blind, randomized controlled trial of dapagliflozin in improving ventricular remodeling in patients with left ventricular dysfunction after acute myocardial infarction

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049019
Enrollment
Unknown
Registered
2021-07-19
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-03-28

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

Conditions

Acute Myocardial Infarction

Interventions

The test group:dapagliflozin is added to the conventional treatment
The control group:the conventional treatment

Sponsors

Hunan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patient with age more than 18 years old and less than 80 years old; 2.Patient is diagnosed with acute myocardial infarction and have already underwent percutaneous coronary intervention; 3.The left ventricular ejection fraction (LVEF) is less than 50% ; 4.Patient is willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Type 1 diabetes; 2. Severe renal insufficiency (eGFR less than 30ml/min/1.73?); 3. Mechanical complications of acute myocardial infarction, such as ventricular septal perforation; 4. Systolic blood pressure less than 100mmHg; 5. Active hematuria or urinary tract infection; 6. SGLT2 inhibitors have been used; 7. Diseases that can affect the NLRP3 inflammasome signaling pathway: obesity (BMI>30kg/?), gout, silicosis, Alzheimer's disease, active hepatitis, malignant tumors, autoimmune diseases such as rheumatoid arthritis , Ankylosing spondylitis, take antioxidant drugs, such as vitamin E; 8. Combined with severe disease with expected survival time of less than 6 months.

Design outcomes

Primary

MeasureTime frame
Left ventricular end-diastolic volume;left ventricular ejection fraction;

Secondary

MeasureTime frame
IL-1ß and IL-18;

Countries

China

Contacts

Public ContactPeng Jianqiang

Hunan Provincial People's Hospital

2925772400@qq.com+86 13507426900

Outcome results

None listed

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