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RECRUITING
NCT05646394

Registry on Augmented Antithrombotic Treatment Regimens for Patients With Arterial Thrombotic APS

Sponsor: McMaster University

View on ClinicalTrials.gov

Summary

The goal of this registry is to gather more information on the efficacy and safety of various antithrombotic regimens. The registry collects data on patients with antiphospholipid syndrome and an arterial event within the past 12 months, on treatment with either A) a VKA with therapeutic range, INR 2.0-3.0 plus low-dose aspirin (75-100 mg daily), B) a VKA alone with therapeutic range, INR 2.0-3.0, C) a VKA with therapeutic range, INR 3.0-4.0, or D) with a dual antiplatelet regimen. The follow-up is 2 years.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

150

Start Date

2022-07-01

Completion Date

2029-12-31

Last Updated

2025-12-09

Healthy Volunteers

No

Interventions

DRUG

Dual antiplatelet therapy

Aspirin plus any of clopidogrel, ticagrelor or prasugrel

DRUG

Combined antithrombotic therapy

Combination of a vitamin K antagonist, such as warfarin, acenocoumarol, phenprocoumon, phenindione etc, with low-dose aspirin.

DRUG

Vitamin K antagonist standard intensity

vitamin K antagonist, such as warfarin, acenocoumarol, phenprocoumon, phenindione etc, with therapeutic range, international normalized ratio 2.0-3.0

DRUG

Vitamin K antagonist high intensity

vitamin K antagonist, such as warfarin, acenocoumarol, phenprocoumon, phenindione etc, with therapeutic range, international normalized ratio 3.0-4.0

Locations (3)

Instituto de Investigaciones en Salud Pública, Universidad de Buenos Aires

Buenos Aires, Buenos Aires F.D., Argentina

Clinica Universitaria Reina Fabiola

Córdoba, Argentina

McMaster University

Hamilton, Ontario, Canada