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NCT05896501Not yet recruiting

Role of FFR in ACS Patients: Pressure ACS Registry

Role of Fractional Flow Reserve Assessment Using Pressure Wire in Patients With Acute Coronary Syndrome Who Treated With Xience Stent; a Multicenter, Prospective, and Observational Registry
The Catholic University of KoreaClinicalTrials.govdeviceDevice trial
Study focus
Drug/Device/Intervention
Fractional Flow Reserve
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
The Catholic University of Korea
Location
Suwon,Uijeongbu,Daejeon,Incheon,Seoul, South Korea
Timeline & enrollment
Phase
N/A
Start date
Jan 01, 2020
End date
Jun 30, 2025
Enrollment
500 participants
Primary outcome

Rate of Major adverse cardiac events

Summary

Currently, fractional flow reserve (FFR) is regarded as a gold-standard invasive method to
 define lesion-specific ischemia and FFR-guided PCI has been proven to reduce unnecessary
 revascularization and to enhance patient's clinical outcomes. Therefore, current guidelines
 recommend FFR measurement for intermediate coronary stenosis when there is no definite
 evidence of lesion-specific ischemia. However, previous evidences which well demonstrated the
 benefit of FFR-guided strategy were mostly generated from patients with stable coronary
 artery disease.4 FFR may be overestimated and the hemodynamic relevance of a coronary
 stenosis underestimated in patients with acute coronary syndrome (ACS).Its role in ACS
 patients still needs to be defined although several studies have recently published
 addressing the value of FFR-guided PCI in ACS. In fact, recent evidence suggests that culprit
 lesions of patients presenting with a non-ST-segment elevation myocardial infarction that
 were deferred based on a negative FFR have a relatively high event rate, calling into
 question the use of FFR in that patient population.

ICD-10 classifications
Acute myocardial infarctionAcute myocardial infarction, unspecifiedAcute subendocardial myocardial infarctionAcute ischaemic heart disease, unspecifiedOther acute ischaemic heart diseases
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05896501
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT05896501 through Pure Global AI's free database. This phase not specified trial is sponsored by The Catholic University of Korea and is currently Not yet recruiting. The study focuses on Acute Coronary Syndrome. Target enrollment is 500 participants.

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