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NOT YET RECRUITING
NCT07898709
PHASE2

Evaluating SGLT2 Inhibitors for the Reduction of No-Reflow Phenomenon in Patients Undergoing PCI

Sponsor: Al-Azhar University

View on ClinicalTrials.gov

Summary

Study Background \& Purpose: The no-reflow phenomenon is a significant complication occurring in patients with acute myocardial infarction who undergo percutaneous coronary intervention (PCI). It leads to poor myocardial perfusion despite successful opening of the culprit coronary artery. Sodium-glucose cotransporter 2 (SGLT2) inhibitors have demonstrated cardioprotective mechanisms beyond glucose control. Objective: This randomized controlled trial aims to evaluate the effectiveness and safety of administering SGLT2 inhibitors as adjunctive therapy in reducing the incidence of the no-reflow phenomenon in patients with myocardial infarction undergoing PCI. Study Plan: Eligible patients presenting with myocardial infarction scheduled for PCI will be randomized into three groups: one group receiving standard pharmacological care plus Empagliflozin therapy, second group receiving standard pharmacological care plus dapagliflozin therapy, and the control group receiving standard pharmacological care alone. Patients will be monitored during and after the procedure to evaluate coronary blood flow and incidence of no reflow phenomenon.

Official title: Evaluation of Sodium-glucose Cotransporter 2 (SGLT2) Inhibitors Administration as Adjunctive Therapies for the Reduction of the No-reflow Phenomenon in Patients With Myocardial Infarction Undergoing Percutaneous Coronary Intervention (PCI): A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2027-01

Completion Date

2027-08

Last Updated

2026-10-27

Healthy Volunteers

No

Interventions

DRUG

Empagliflozin (SGLT2i)

Patients will receive standard guideline-directed treatment in accordance with current clinical guidelines in addition to empagliflozin orally as a single oral dose before PCI, followed by empagliflozin orally once daily for three days.

DRUG

dapagliflozin

Patients will receive standard guideline-directed treatment in accordance with current clinical guidelines in addition to dapagliflozin orally as a single oral dose before PCI, followed by dapagliflozin orally once daily for three days.

DRUG

Standard medical treatment

Patients will receive standard guideline-directed treatment in accordance with current clinical guidelines and undergo percutaneous coronary intervention without receiving any study medication.

Locations (4)

Al Hussein University Hospital

Cairo, Egypt

Al-Zahraa University Hospital

Cairo, Egypt

Islamic Cardiac Surgery Center , Al-Azhar University

Cairo, Egypt

Sayed Galal University Hospital

Cairo, Egypt