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Predictive Value of Combining AccuIMR and AccuFFR in Patients With STEMI

Predictive Value of Combining Angio-Based Index of Microcirculatory Resistance and Fractional Flow Reserve in Patients With STEMI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06435728
Enrollment
1297
Registered
2024-05-30
Start date
2024-03-01
Completion date
2024-05-30
Last updated
2024-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute ST Segment Elevation Myocardial Infarction, Prognosis

Brief summary

Patients with acute myocardial infarction were enrolled retrospectively. The fractional flow reserve (AccuFFR) and microcirculatory resistance index (AccuIMR) based on coronary angiography were analyzed, and the relationship between FFR and IMR and the prognosis of patients with acute myocardial infarction was analyzed

Detailed description

We retrospectively enrolled STEMI patients who underwent PCI in Peking University Third Hospital. The fractional flow reserve (AccuFFR) and microcirculatory resistance index (AccuIMR) based on coronary angiography were obtained by analyzing the coronary angiography images. The prognosis of patients was obtained by searching inpatient and outpatient systems and telephone follow-up. The relationship between AccuFFR, AccuIMR and prognosis was statistically analyzed

Interventions

DIAGNOSTIC_TESTAccuIMR and AccuFFR

AccuFFR and AccuIMR were obtained by reviewing coronary angiography at the time of primary PCI

Sponsors

Peking University Third Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age of \>18 years; * Onset-to-treatment time of ≤12 h, meeting the diagnostic criteria for STEMI; * underwent primary PCI within 12 h of symptom onset and achieved successful PCI in the culprit vessel; * Availability of complete clinical data

Exclusion criteria

* severe tortuosity and overlap of the target vessel; * poor-quality coronary angiography images; * missing two coronary angiography images \>25° apart

Design outcomes

Primary

MeasureTime frameDescription
MACE3 years after myocardial infarctioncardiovascular death, all-cause death, readmission for heart failure (HF), and recurrent coronary events

Secondary

MeasureTime frameDescription
recurrent coronary events3 years after myocardial infarctionnonfatal myocardial infarction, unplanned PCI, and unplanned coronary artery bypass grafting

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026