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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04582175
Other study ID # Uoradea
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2020
Est. completion date September 5, 2020

Study information

Verified date October 2020
Source University of Oradea
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study aimed to compare major adverse cardiac and cerebrovascular events(MACCE) and mortality at one year between two strategies: complete revascularization including non-culprit lesions percutaneous coronary intervention(PCI) during primary PCI(PPCI) versus complete revascularisation during the same hospital admission in multi-vascular coronary artery disease(MVD) patients presenting with ST-elevation myocardial infarction(STEMI) uncomplicated by cardiogenic shock.


Description:

Complete revascularisation in MVD patients with STEMI uncomplicated by cardiogenic shock has been shown to improve outcomes, however the optimal timing of treatment of the non-culprit lesions is not known. The 2018 ESC/EACTS Guidelines on myocardial revascularization states that "routine revascularization of non-IRA (infarct related artery) lesions should be considered in patients with multivessel disease before hospital discharge". Our trial showed that among the fore mentioned patients there was no difference regarding outcomes when using a strategy of complete revascularization with non-culprit lesions PCI during PPCI or during the same hospital admission.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date September 5, 2020
Est. primary completion date September 1, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

1. Men and women with successful PCI (preferably using a drug-eluting stent) to the culprit lesion for STEMI ( PCI for STEMI should be primary PCI in the first 12 hours after symptom onset) and complete revascularization of non-culprit lesions during the index PPCI procedure or during a different procedure performed before index hospital discharge.

2. Multi-vessel disease defined as at least 1 additional non-infarct related coronary artery lesion that is at least 2.5 mm in diameter that has not been stented as part of the primary PCI and that is amenable to successful treatment with PCI and has:

- At least 75% diameter stenosis (visual estimation) or

- At least 50% diameter stenosis (visual estimation) with fractional flow reserve (FFR) = 0.80

3. Age between 18 and 90 years

4. Written informed consent could be obtained from all the patients

Exclusion Criteria:

1. Rescue PCI for failed fibrinolysis or a combination strategy where PCI is performed routinely 3-12 hours after fibrinolysis

2. Cardiogenic shock

3. Non-cardiovascular known co-morbidity reducing life expectancy to < 2 years

4. Any factor precluding 1year follow-up

5. Prior Coronary Artery Bypass Graft (CABG) Surgery

6. A different operator from the previously designated

7. Unable to provide consent for any other reason

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
angioplasty
angioplasty of all non-culprit lesions

Locations

Country Name City State
Romania Spitalul Clinic Judetean de Urgenta Oradea Oradea Bihor

Sponsors (1)

Lead Sponsor Collaborator
University of Oradea

Country where clinical trial is conducted

Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary one year all-cause mortality death at one year one year
Primary MACCE at one year major adverse cardiac and cerebrovascular events including cardiac death, stroke, symptom-driven revascularization, myocardial infarction one year
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