Last updated: April 19, 2024
Sponsor: Korea University Anam Hospital
Overall Status: Active - Not Recruiting
Phase
N/A
Condition
Occlusions
Congestive Heart Failure
Heart Disease
Treatment
Immediate stenting
Deferred stenting
Clinical Study ID
NCT03744000
INNOVATION-CORE
Ages 19-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Typical ischemic chest pain lasting more than 30 minutes
- New ST elevation at the J point in two contiguous leads with the cut-points: ≥0.1 mVin all leads other than leads V2-V3 where the following cut-points apply: 0.2 ≥mV inmen ≥40 years; ≥0.25 mV in men <40 years, or ≥0.15 mV in women27 or new left bundlebranch block28.
- Symptom onset of chest pain within 6 hours
- If left anterior descending artery is culprit lesion on coronary angiography (Ostiumto mid lesion). However, if the right coronary artery is hypoplastic and the distalportion of the left anterior descending artery feeds to the area of the posteriorlower coronary artery (PDA), culprit lesion of the distal part of left anteriordescending artery can also be included in the study.
- If TIMI blood flow before intervention is 0, 1 or 2
- If TIMI 3 blood flow was secured before coronary stenting by intracoronary abciximabinjection, manual thrombus aspiration and balloon dilatation
- Patients who wrote the informed consent: The subject should be able to receiveinformations of treatment, risks, effects and other therapeutic modalities regardingstaged percutaneous coronary intervention (PCI) at least verbally, and investigatorsshould be provided written informed consent from a subject or a legally recognizedrepresentative prior to giving any treatment related to the study.
Exclusion
Exclusion Criteria:
- If there is a previous history of myocardial infarction or coronary artery bypasssurgery
- Cardiogenic shock
- Rescue PCI after thrombolytic therapy
- If the life expectancy of the accompanying disease is expected to be less than oneyear or the patient is not cooperating with the protocol.
- In cases where the left main lesion is an infarction related artery (If the left mainlesion is a simple left main branch lesion rather than an infarction related vessel,it is included in the study)
- STEMI due to Stent thrombosis
- A major dissection (Type C to F) occurred during the procedure including balloondilatation for securing TIMI blood flow and the risk of acute closure at the time ofstaged stenting was expected
Study Design
Total Participants: 185
Treatment Group(s): 2
Primary Treatment: Immediate stenting
Phase:
Study Start date:
April 03, 2018
Estimated Completion Date:
November 30, 2025
Study Description
Connect with a study center
Korea University Anam Hospital
Seoul, 02841
Korea, Republic ofSite Not Available
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