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Cardiovascular Registry of Atrial Fibrillation

Cardiovascular Registry of Atrial Fibrillation in Latin America: The LACROSS Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04456842
Acronym
LACROSS
Enrollment
2016
Registered
2020-07-07
Start date
2020-08-04
Completion date
2024-09-30
Last updated
2024-10-04

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

Conditions

Atrial Fibrillation, Atrial Flutter

Keywords

Atrial Fibrilation, Antithrombotic therapy, Atrial Flutter

Brief summary

Follow a representative sample of Latin American patients diagnosed with atrial fibrillation to set data on demographic characteristics, documenting antithrombotic therapy, describe the INR control level of VKA users, discontinuation rates and clinical outcomes, such as stroke, hemorrhage and death

Detailed description

Patients will be followed 6 months and 1 year after the baseline visit and will be collected data of antithrombotic therapy, laboratory data, discontinuation rates of antithrombotic therapy and clinical outcomes.

Interventions

OTHERPatient Registry Data

To set data on demographic characteristics,documenting antithrombotic therapy, describe the INR control level of VKA users, discontinuation rates and clinical outcomes, such as stroke, hemorrhage and death.

Sponsors

Brazilian Clinical Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age \> 18 years-old that signed informed consent; * Atrial Fibrillation or Atrial Flutter at the time of inclusion documented in source document; * If the patient is not in atrial fibrillation or Atrial Flutter rhythm, s/he should have 2 electrographic records, at least 15 days apart between them, with one of them being performed within the last 6 months before enrollment (AF may be documented by 12-lead ECG, Holter monitor-24h);

Exclusion criteria

* Patients who did not agree to participate. * Patients without possibility of monitoring for one year.

Design outcomes

Primary

MeasureTime frame
INR control rate12 months
Oral anticoagulation discontinuation rate12 months
Percentage of death12 months
Percentage of stroke12 months
Percentage of systemic embolism12 months
Percentage of myocardial infarction12 months
Percentage of major bleeding12 months
Percentage of electrical cardioversion12 months
Percentage of percutaneous ablation of AF12 months
Percentage of atrioventricular junction ablation12 months
Percentage of patients that need of pacemaker implantation12 monts
Percentage of other cardiovascular hospitalization12 months

Countries

Argentina, Brazil, Colombia, Mexico

Outcome results

None listed

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