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Culprit-first in Primary Percutaneous Coronary Intervention

Culprit-first Versus Culprit-last Approach During Primary Percutaneous Coronary Intervention in Patients With ST-elevation Myocardial Infarction: A Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05415085
Enrollment
106
Registered
2022-06-10
Start date
2021-05-01
Completion date
2023-04-13
Last updated
2023-10-19

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

Conditions

Coronary Artery Disease, Ischemic Heart Disease, Myocardial Infarction, STEMI, Stent

Keywords

coronary artery disease, STEMI, primary PCI, door-to-balloon time

Brief summary

The aim of this study is to assess the impact of culprit-first versus culprit-last percutaneous coronary intervention on the door to balloon time and clinical outcomes in patients with ST-elevation myocardial infarction.

Detailed description

Ischemic heart disease (IHD) is the single most common cause of death and its frequency is increasing globally. It is estimated that IHD is the cause of 1.8 million deaths or 20% of all deaths in Europe. Despite advancements in the fields of rapid diagnosis and in treatment strategies, the morbidity, and mortality in patients with ST-segment myocardial infarction remains substantial, with an estimated mortality rate of 4-12% according to registries of the ESC countries. According to the 2017 European Society of Cardiology (ESC) guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation (STEMI), there is a level 1 recommendation with a level of evidence A for primary percutaneous coronary intervention (PPCI) strategy in patients with STEMI, and this strategy is preferred over fibrinolytic therapy. In addition, the ESC guidelines recommend a first medical contact to reperfusion time within 60 minutes in STEMI patients for primary PCI-capable centers. This recommendation is supported by a recently published study that showed shortening door to balloon (D2B) time was significantly associated with survival benefit. Based on the recommendation for maximal D2B time in STEMI patients to be 60 minutes, many countries and institutions worldwide have established programs, among them the national program for quality indicators by the Israeli ministry of health, to shorten D2B times. According to data published by the Israeli ministry of health in the year 2018, 88% of STEMI patients had a D2B time of \<90 minutes. The common practice during PPCI is to complete diagnostic angiography of the whole coronary tree before performing culprit-vessel revascularization. This practice is not evidence-based and current guidelines do not prioritize full diagnostic angiography over culprit-vessel revascularization first. As was found in previous studies, this practice might result in delaying revascularization by 4-8 minutes in D2B time. This delay might potentially lead to worse outcomes in STEMI patients, although not proven in the above-cited studies.

Interventions

PROCEDURECulprit-first PCI

PCI to the culprit artery prior to the demonstration of the whole coronary tree.

Sponsors

Shaare Zedek Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

* Patients presenting with STEMI who are eligible for PPCI

Exclusion criteria

* Cardiac arrest * Cardiopulmonary resuscitation or extracorporeal membrane oxygenation on arrival to the catheterization laboratory * Prior coronary artery bypass grafting surgery

Design outcomes

Primary

MeasureTime frameDescription
Needle-to-balloon time of 10 minutes or lessthrough study completion, an average of 1 yearChange in needle-to-balloon time in minutes

Secondary

MeasureTime frameDescription
Need for hemodynamic (mechanical/medical) support during PCIthrough study completion, an average of 1 yearNumber of patients that needed mechanical support during PCI
Need for respiratory support during PCIthrough study completion, an average of 1 yearNumber of patients that needed respiratory support during PCI
Rate of failed PCIthrough study completion, an average of 1 yearAs determined by the operator

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026