LATAM Bif Registry
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 →
Unsure about the terms? Read our patient guide →
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