tirofiban
Drugtirofiban (25 μg/kg bolus and 0.15 μg/kg/min maintenance infusion for 24 hours)
NCT Number: NCT00611169
The purpose of this study to investigate whether the administration of high-dose tirofiban before primary PCI could reduce myocardial infarct size, using analysis of contrast-enhanced magnetic resonance imaging.
Looking for future studies?
Notify Me18 year–80 year
All sexes
Interventional
Phase 4
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
tirofiban (25 μg/kg bolus and 0.15 μg/kg/min maintenance infusion for 24 hours)
Time frame: within the first 30 days after index procedure
Time frame: at 6 month after index procedure
Samsung Medical Center
Other
The Effects of Facilitated Percutaeous Coronary Intervention Compared to Primary Percutaneous Coronary Intervention in Patients With ST-Segment Elevation Acute Myocardial Infarction
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05511649
Acute Myocardial Infarction, Cardiovascular Diseases
Kaifeng, Henan, China
View Trial DetailsNCT06463275
Acute Myocardial Infarction, Cardiovascular Diseases
Mölndal, Gothenburg, Sweden
View Trial DetailsNCT06499519
Acute Myocardial Infarction, Cardiovascular Diseases
Aarhus, Denmark
View Trial DetailsNCT00727623
Acute Coronary Syndrome, Acute Myocardial Infarction
La Louvière, Hainaut, Belgium
View Trial Details