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Not yet recruiting NCT04471883

LATAM Bif Registry

Observational Coronary Bifurcation Lesion

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Percutaneous coronary interventions.
Who it may be relevant to
Registry conditions: Coronary Bifurcation Lesion. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Latin American Registry of Percutaneous Interventions in Coronary Bifurcations

Overview

The LATAM Bif Registy is an international and prospective registry of percutaneous coronary interventions (PCI) in coronary bifurcation lesions. The main goal of the study is to investigate the current state and long-term outcomes of PCI in this complex subset of coronary lesions in Latin America.

Interventions

  • Procedure Percutaneous coronary interventions
    Percutaneous coronary interventions in coronary bifurcation lesions

Primary outcome measures

  • Cardiac Death [Time frame: 5 years]
  • Myocardial Infarction [Time frame: 5 years]
  • Target Lesion Revascularization [Time frame: 5 years]
  • Stent thrombosis [Time frame: 5 years]
  • Major bleeding [Time frame: 5 years]

Eligibility criteria

Inclusion criteria

  • Age >= 18 years
  • Any type of bifurcation lesion
  • Side-branch reference diameter >= 2 mm

Exclusion criteria

  • Protected left main disease in patients with previous CABG
  • Patients who refuse to be included in the registry

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT04471883 · 00543186

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗