Reperfusion Approach in Predicted In-hospital Delay for Primary PCI in STEMI
Starting soon · Phase 4
Conditions studied: STEMI - ST Elevation Myocardial Infarction
In brief
This study aims at evaluating of the effectiveness of in-hospital thrombolysis for ST-segment elevation myocardial infarction in PCI centers under conditions of predicted in-hospital delay (\>60 min after admission in PCI-center) of PCI. Following randomisation a strategy of early tenecteplase and additional antiplatelet and antithrombin therapy followed by catheterisation within 2-24 hours with timely coronary intervention as appropriate (or by rescue coronary intervention if required) in Group A will be compared to primary PCI performed according to local standards in Group B.
Key facts
- Study ID
- NCT07641231
- Run by
- National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
- People needed
- 240
- Starts
- 2026-05-20
- Expected to finish
- 2029-05-20
- Last updated by the study team
- 2026-06-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age equal or greater than 18 years
- "Symptom onset-randomization" time interval <12 hours
- Predicted "diagnosis-pPCI" time interval equal or greater than 120 minutes
- Predicted "admission-pPCI" time interval equal or greater than 60 minutes
- Informed consent received
You may not qualify if…
- Medical history, procedures, medication administration or the presence of factors that would in general predispose to bleeding events and/or the inability to evaluate the study primary endpoint
Where it is running
- National Medical Research Center for Cardiology, Ministry of Health of Russian Federation — Moscow, Select A State, Russia
Full record on ClinicalTrials.gov
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