Not a traditional drug phase: testing Dapagliflozin 10mg Tab for Myocardial Infarction
This study aims to investigate the effect of early administration of DAPA during ischemia and before pPCI on infarct size, reperfusion injury-related myocardial damage, cardioprotection from HF, and renoprotection from AKI in patients with AMI.
Official registry: https://clinicaltrials.gov/study/NCT06009874 · Mohammad Hussien Tantawy Soliman · enrollment listed as 80
What this phase means
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are Dapagliflozin 10mg Tab, or Placebo. The registry lists allocation as randomized. This study aims to investigate the effect of early administration of DAPA during ischemia and before pPCI on infarct size, reperfusion injury-related myocardial damage, cardioprotection from HF, and renoprotection from AKI in patients with AMI.
They plan to enroll about 80 people at Shibīn al Kawm. Taking part typically means taking a study drug (or dummy pill) plus check-ins.
Official title (unrewritten)
Clinical Investigation of Cardioprotective Effect of Early Administration of Sodium-glucose Cotransport-2 Inhibitors in Patients With Acute Myocardial Infarction
Interventions: Dapagliflozin 10mg Tab, Placebo
Primary outcome (registry wording): difference in infarct size
Who it is for (from inclusion criteria)
- Ages 18 Years to 80 Years
- Patients with ST-elevation myocardial infarction (STEMI)
- STEMI was defined according to the Fourth Universal Definition of AMI
- 18 - 80 years of age
- Diabetics or non-diabetics
- eGFR \> 45 ml/min/1.73m2
- Blood pressure before first drug dosing \>110/70 mmHg
Who the registry excludes
- History of diabetic ketoacidosis
- Genital and urinary infections
- Previous coronary artery bypass surgery
- Severe hepatic insufficiency
- Advanced cancer patients
- Known allergy to SGLT-2 inhibitors
- Hemodynamic instability
Public study contact (from the registry)
Mohammad Soliman
Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.
Sites listed on ClinicalTrials.gov
1 listed- Mohammad Soliman — Shibīn al Kawm, Menofia, Egypt (recruiting)
FAQ about this NCT record
Is NCT06009874 still recruiting?
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT06009874?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT06009874?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.
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