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Innate Immune Cell Phenotypes and Early Fibrotic Repair in Acute Myocardial Infarction

Innate Immune Cell Phenotypes and Early Fibrotic Repair in Acute Myocardial Infarction

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07764588
Acronym
ICE-AMI
Enrollment
50
Registered
2026-08-14
Start date
2026-01-01
Completion date
2026-12-31
Last updated
2026-08-14

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

Conditions

Myocardial Infarction

Keywords

neutrophil, monocyte, myocardial infarction, cardiac remodeling, cardiac magnetic resonance

Brief summary

To determine the relationship of the phenotypes of neutrophils and monocytes with early fibrotic repair after acute myocardial infarction.

Detailed description

This study will enroll 50 patients with ST-segment elevation myocardial infarction (STEMI). Peripheral blood will be collected from these patients for immune cell subset analysis, serum cytokine evaluation, and neutrophil sorting for transcriptome sequencing. At 1 week after admission, cardiac magnetic resonance (CMR) will be performed to evaluate the myocardial salvage index, area of late gadolinium enhancement (LGE), microvascular obstruction (MVO), extracellular volume (ECV), and left ventricular ejection fraction (LVEF).

Interventions

None listed

Sponsors

Shanghai 10th People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

\---- Age \> 18 and ≤ 80 years old \- Patients with acute STEMI within 12 hours of symptom onset who are planned to receive PPCI

Exclusion criteria

* Prior revascularization * Known allergy to gadopentetate dimeglumine contrast agent * Pregnancy or planned pregnancy within the next 6 months * Life expectancy \< 1 year * Metallic implants or claustrophobia that precluded MRI * Severe COPD or inability to hold breath for MRI * Severe hepatic or renal dysfunction (ALT \> 5×ULN or eGFR \< 15 mL/min/1.73 m²)

Design outcomes

Primary

MeasureTime frameDescription
Major cardiac adverse outcomeAt 12 months after enrollmentThe composite endpoint included cardiac death, non-fatal myocardial infarction, and rehospitalization for angina.

Secondary

MeasureTime frameDescription
Cardiac remodeling measured by CMRAt 1 week after admissionCMR will be performed to evaluate the cardiac fibrosis defined as area of late gadolinium enhancement (LGE).

Countries

China

Contacts

CONTACTJianhui Zhuang, MD
jh_zhuang@tongji.edu.cn86-13621742833

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026