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Prognostic Value of the CALLY Index in Patients Undergoing Primary PCI

Prognostic Value of the C-Reactive Protein-Albumin-Lymphocyte (CALLY) Index on Patients Undergoing Primary Percutaneous Coronary Intervention

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07203573
Enrollment
140
Registered
2025-10-02
Start date
2025-09-25
Completion date
2026-10-25
Last updated
2025-10-02

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

Conditions

Primary Percutaneous Coronary Intervention

Brief summary

This study aims to evaluate the relationship between the admission CALLY index and short-term adverse outcomes in STEMI patients undergoing PPCI. Specifically, it seeks to determine whether the CALLY index is associated with in-hospital and 30-day complications, including heart failure, arrhythmias, reinfarction, or death. Additionally, the study will assess the association between the CALLY index and procedural success, defined by post-intervention TIMI flow, as well as the complexity of coronary artery disease using the SYNTAX score.

Detailed description

* ST-elevation myocardial infarction (STEMI) remains a leading cause of morbidity and mortality worldwide. Early risk stratification in patients undergoing primary percutaneous coronary intervention (PPCI) is crucial to predict adverse outcomes and optimize management. * The C-reactive protein-albumin-lymphocyte (CALLY) index is an emerging biomarker combining inflammation, nutrition, and immune status. Previous studies have demonstrated associations between the CALLY index and long-term mortality in cardiovascular disease, elderly populations, and STEMI patients . However, most of these studies focus on long-term outcomes or utilize complex predictive models (e.g., machine learning), and there is limited research assessing the direct relationship between admission CALLY index and immediate procedural outcomes, such as PPCI success or short-term adverse events., Unlike previous studies that included retrospective data, large national databases, or machine learning prediction models, this study will focus on a short-term, real-time assessment of the CALLY index at admission and its immediate association with procedural outcomes and in-hospital adverse events

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

Age ≥ 18 years * Diagnosis of STEMI based on 4th universal definition of myocardial infarction * Undergoing Primary PCI within guideline-recommended timeframes * Provided informed consent to participate in the study

Exclusion criteria

* Active infection (as detected by baseline leukocytosis on admission), autoimmune or inflammatory disease affecting CRP, albumin, or lymphocyte counts * Chronic liver disease or advanced malignancy * Patients receiving immunosuppressive therapy * Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Short-term major adverse cardiac events (MACE)Through hospital stay (up to 3 days) and at one-month follow-up post-intervention.Occurrence of MACE including heart failure, arrhythmias, reinfarction, cardiogenic shock, or death.

Secondary

MeasureTime frameDescription
Procedural success of PPCIImmediately post-procedureAchievement of final TIMI 3 flow grade post-intervention without in-hospital complications.
Coronary artery disease complexity by SYNTAX score ( (Synergy Between PCI With Taxus and Cardiac Surgery score)At the time of coronary angiographyAssessment of the association between CALLY index at admission and coronary complexity determined by the SYNTAX (Synergy Between PCI With Taxus and Cardiac Surgery) score. The SYNTAX score ranges from 0 upwards, with scores categorized as 0-22 indicating low complexity and scores \>22 indicating more complex coronary artery disease. Higher scores represent increased disease complexity.

Contacts

Primary ContactMadona S Anis
Madona.17289597@med.aun.edu.eg+20 109 179 1874

Outcome results

None listed

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