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Active, not recruiting Observational

Effect of Genetic Polymorphism on the Clinical Outcome to SGLT2 Inhibitors in Heart Failure Patients

NCT06901609 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2023-11-22
Last updated
2025-03-30

Condition(s) studied

Heart Failure - NYHA II - IVCardiac FibrosisCardiac Remodeling

Investigational drug(s) / intervention(s)

SGLT2 inhibitor (Dapagliflozin 10mg) →

SGLT2 inhibitor (Dapagliflozin 10mg): Renal response after 6 months of Dapagliflozin therapy among patients with heart failure reduced ejection fraction.

Study summary

Heart failure with reduced ejection fraction (HFrEF) is a significant cause of morbidity and mortality. Sodium-glucose co-transporter-2 (SGLT2) inhibitors have demonstrated efficacy in improving renal outcomes in patients with HFrEF. Pharmacogenetics, the study of how genetic variations influence drug response, could elucidate inter-individual variability in treatment outcomes. This study aims to assess the impact of specific genetic variants on renal outcomes in HFrEF patients treated with SGLT2 inhibitors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (≥18 years) with HFrEF (LVEF ≤40%). * Initiation of SGLT2 inhibitor therapy. * Stable background HF therapy for at least 4 weeks. * Written informed consent for participation and genetic testing. Exclusion Criteria: * Known hypersensitivity to SGLT2 inhibitors. * History of ketoacidosis or recurrent urinary tract infections. * End-stage renal disease (eGFR \<30 mL/min/1.73 m²). * Life expectancy \<6 months due to non-cardiovascular conditions. * Pregnancy or lactation.

Primary outcome measure(s)

  • Reno-protective effect and gene polymorphism — 6 months
    Association between genetic polymorphism in SLC5A2, UMOD and ACE and Renal response in-terms of change in GFR among patients with heart failure.

Trial sites (1)

FacilityCityRegionStatus
National Heart Institute Cairo Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06901609 on ClinicalTrials.gov ↗ ← All trials in Egypt