Pressure-Flow Measurements Directly after Primary PCI to Predict Late Occurrence of Microvascular Obstructio
Completed
- Conditions
- myocardial infarction10011082
- Registration Number
- NL-OMON38350
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
- Patients with acute STEMI
- Presentation at catheterization laboratory within 6 hours after onset of symptoms
Exclusion Criteria
- previous myocardial infarction in the same artery
- significant three-vessel disease (lesions >70%)
- unsuccessful primary PCI
- refusal or inability to give informed consent
- contra indications for abciximab
- cardiogenic shock
- poor kidney function, eGFR < 30 mg/ml/min
-extreme fear and chestpain
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>resistance measurements using combowire<br /><br>thermodilution measurements using the PressureWire Certus</p><br>
- Secondary Outcome Measures
Name Time Method <p>MRI scan<br /><br>PET scan<br /><br>blood measurements</p><br>