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Treatment Pattern of NOACs (Non-vitamin K Oral Anticoagulants) in Outpatient Users in Colombian Databases

Treatment Pattern of NOACs (Non-vitamin K Oral Anticoagulants) in Outpatient Users in Colombian Databases - TREND Colombia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03474757
Acronym
TREND
Enrollment
10528
Registered
2018-03-23
Start date
2018-02-28
Completion date
2018-07-30
Last updated
2020-10-06

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

Conditions

Atrial Fibrillation

Brief summary

This population-based descriptive study will characterize first-time users of three NOACs (rivaroxaban, dabigatran and apixaban) in prevention of stroke in non-valvular atrial fibrillation (SPAF) patients and will assess the patterns of drug utilization in routine general practice in Colombia

Interventions

OTHERData Collection

Data will be extracted from July 2009 to the last available database extraction

Sponsors

Janssen Research & Development, LLC
CollaboratorINDUSTRY
Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* First prescription of NOACs (rivaroxaban, dabigatran and apixaban) in the outpatient setting. * Non valvular Atrial Fibrillation (NVAF) Patients * aged ≥18 years * at least one year of enrollment in the Audifarma database * one year since first encounter with healthcare provider will be included in the study

Exclusion criteria

* Patients with any record of index drug prescription prior to the enrolment period. * Patients who qualify as members of more than one cohort study on the same day

Design outcomes

Primary

MeasureTime frameDescription
Switch to another study drugUp to 6 years
AgeAt Baseline
SexAt Baseline
Co-morbidityAt Baseline
Healthcare utilizationUp to 2 yearsPrimary Care Physicians visits, Outpatient visits and Hospital admissions
Proportion of Naive to non-naive patientAt Baseline
Dose at first prescriptionUp to 6 years
Duration of treatmentUp to 6 years
DiscontinuationUp to 6 years

Secondary

MeasureTime frame
Time trends of usage of study medicationsUp to 6 years

Countries

Colombia

Outcome results

None listed

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