NOAC Portuguese Real World Study

NCT04808934 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2023-04-05

No results posted yet for this study

Summary

To determine if there is any difference in the effectiveness and safety outcomes of patients with NVAF newly treated with apixaban, dabigatran, rivaroxaban and vitamin K antagonists

Conditions

  • Stroke
  • Systemic Embolism
  • Major Bleeding

Interventions

DRUG

Apixaban

Adults receiving apixaban

DRUG

dabigatran

Adults receiving dabigatran

DRUG

rivaroxaban

Adults receiving rivaroxaban

DRUG

VKAs

Adults receiving VKA

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-01
Primary Completion
2020-12-01
Completion
2020-12-01
FDA Drug
Yes

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04808934 on ClinicalTrials.gov