MedPath

Postconditioning Rotterdam Trial

Recruiting
Conditions
myocardial infarction, primairy PCI, STEMI, thrombectmy, postconditioning, MRI
Registration Number
NL-OMON26072
Lead Sponsor
Felix Zijlstra, MD, PhD and Olivier Manintveld, MD, PhD (Thoraxcenter, Erasmus MC, Rotterdam, the Netherlands)
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
72
Inclusion Criteria

Patients are included in the study when written informed consent is given. Consecutive patients as defined above are screened for inclusion in the trial. The eligibility criteria consist of the following:

1. Delay between onset of chest pain and PCI ≤ 6 hours in case of inferiolateral wall infarction and ≤ 12 hours in case of anterior wall infarction;

Exclusion Criteria

1. Younger than 18 or older than 75 years of age;

2. Cardiogenic shock defined as sustained systolic blood pressure ≤ 80 mmHg despite fluid hydration and/or the inability to discontinue vasopressors in less than 1 hour before;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Difference of myocardial infarct size between treatment groups measured on delayed enhance (DE) MRI at 3 months.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath