NCT07086807

Brief Summary

Aim of this study is to determine the prevalence, predictors, and impact of total occlusion of the infarct-related coronary artery (IRA) on short-term mortality.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2011

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2011

Completed
8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2019

Completed
5.6 years until next milestone

First Submitted

Initial submission to the registry

July 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 25, 2025

Completed
Last Updated

July 25, 2025

Status Verified

July 1, 2025

Enrollment Period

8 years

First QC Date

July 18, 2025

Last Update Submit

July 18, 2025

Conditions

Acute Myocardial Infarction (AMI)

Keywords

myocardial infarcioninfarct related artery

Outcome Measures

Primary Outcomes (1)

  • Mortality

    Death due to all reasons in a period od 12 months after myocardial infartion

    12 months

Study Arms (2)

Patients with occluded IRA

Patients with acute occlusion (TIMI 0) of the infarct-related artery (IRA) at the time of the coronary intervention due to acute myocardial infartion

Patients with patent IRA

Patients with acute non-occlusion (TIMI 1-3) of the infarct-related artery (IRA) at the time of the coronary intervention due to acute myocardial infartion

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients treated with PCI for AMI at the University Hospital Centre Sestre milosrdnice, Zagreb, Croatia between 2011 and 2018.

You may qualify if:

  • patients treated with PCI for AMI

You may not qualify if:

  • treated without PCI,
  • diagnosed with myocardial infarction with non-obstructive coronary arteries (MINOCA),
  • underwent surgical revascularization (coronary artery bypass grafting).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
12 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD, PhD, cardiologist

Study Record Dates

First Submitted

July 18, 2025

First Posted

July 25, 2025

Study Start

January 1, 2011

Primary Completion

December 31, 2018

Study Completion

December 31, 2019

Last Updated

July 25, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share