IMPRESS in Severe Shock.
Recruiting
- Conditions
- acute myocardial infarctioncardiogenic shock
- Registration Number
- NL-OMON24829
- Lead Sponsor
- Academic Medical Center, Departement of Cardiology
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 48
Inclusion Criteria
1. Delay between onset of chest pain and PCI ≤ 24-72 hours;
2. Cardiogenic shock defined as: systolic blood pressure ≤ 90 mmHg for > 30 minutes or the need for supportive measures to maintain a systolic blood pressure ≥ 90 mmHg;
Exclusion Criteria
1. Severe aorta-iliac arterial disease impeding placement of either devices;
2. Known severe cardiac aortic valvular disease;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 30-day mortality rate.
- Secondary Outcome Measures
Name Time Method 1. Mortality after 6 months, and at 1 to 5 years of follow up;<br /><br>2. Composite of death and severe acquired disability after 6 months, and at 1 to 5 years of follow up.