Overview
SONOthrombolysis in Patients With an ST-segment Elevation Myocardial Infarction With fibrinoLYSIS (SONOSTEMI-LYSIS) Trial
Status:
Recruiting
Recruiting
Trial end date:
2023-05-01
2023-05-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This study will assess the safety and feasibility of sonothrombolysis in the acute management of STEMI undergoing reperfusion therapy with systemic fibrinolysis as part of a pharmacoinvasive approachPhase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of AlbertaCollaborator:
Canadian VIGOUR Centre
Criteria
Inclusion Criteria:- Patients presenting with STEMI within 6 hours of symptom onset and:
1. Are expected to receive reperfusion therapy with fibrinolysis
2. Have a high-risk STEMI ECG as defined as:
- >2mm ST-segment elevation in 2 anterior or lateral leads; or
- >2mm ST-segment elevation in 2 inferior leads coupled with ST-segment
depression in 2 contiguous anterior leads for a total ST-segment deviation
of >4mm
3. Age >30 years
4. Adequate apical and/or parasternal images by echocardiography
Exclusion Criteria:
- 1. Isolated inferior STEMI without anterior ST-segment depression 2. Previous coronary
bypass surgery 3. Cardiogenic shock 4. Known or suspected hypersensitivity to
ultrasound contrast agent used for the study 5. Life expectancy of less than two
months or terminally ill 6. Known bleeding diathesis or contraindication to
glycoprotein 2b/3a inhibitors, anticoagulants, or aspirin 7. Known large right to left
intracardiac shunts 8. Patient received another investigational medication or
treatment within 30 days prior to presentation with STEMI