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Effect and Safety of Fexofenadine Hydrochloride vs Placebo in Patients With Acute Myocardial Infaction: A Randomized Clinical Trial
The purpose of this study was to evaluate the efficacy and safety of fexofenadine hydrochloride on the basis of standard treatment after PCI in STEMI patients.
Details
| Lead sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University |
|---|---|
| Phase | Phase 2 |
| Status | NOT_YET_RECRUITING |
| Enrolment | 165 |
| Start date | 2024-09 |
| Completion | 2026-09 |
Conditions
- ST-segment Elevation Myocardial Infarction (STEMI)
Interventions
- Fexofenadine Hydrochloride 60mg bid
- Placebo
- Fexofenadine Hydrochloride 120mg bid
Primary outcomes
- Late gadolinium enhancement/Left ventricular mass (LGE/LV%) — 6 months after myocardial infarction
LGE/LV% will be assessed by CMR