NOAC Portuguese Real World Study
NCT04808934 · Status: WITHDRAWN · Type: OBSERVATIONAL
Last updated 2023-04-05
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
- lead INDUSTRY
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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