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NCT02161965: VICTORIA

Vascular CalcIfiCation and sTiffness Induced by ORal antIcoAgulation

Completed Phase 4 Last updated 7 November 2019
What this trial tests

Phase 4 trial testing Rivaroxaban in Permanent Atrial Fibrillation in 51 participants. Completed in 16 February 2018.

Timeline
21 May 2013
Primary endpoint
31 December 2016
16 February 2018

Quick facts

Lead sponsorUniversity Hospital, Angers
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment51
Start date21 May 2013
Primary completion31 December 2016
Estimated completion16 February 2018
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Angers

Who can join

18 and older, any sex, with Permanent Atrial Fibrillation or Venous Thrombosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The VICTORIA Study (Vascular CalcIfiCation and sTiffness induced by ORal antIcoAgulation) is a comparative, parallel, prospective, controlled and randomized study of the structural and functional impact of rivaroxaban versus anti-vitamin K drugs on the arterial vasculature.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The effects of vitamin K supplementation and vitamin K antagonists on progression of vascular calcification: ongoing randomized controlled trials.
    Caluwé R, Pyfferoen L, De Boeck K, De Vriese AS. · · 2016 · cited 63× · PMID 26985380 · DOI 10.1093/ckj/sfv146

Verify or expand the search:

Other trials of Rivaroxaban

Trials testing the same drug.

Other University Hospital, Angers trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02161965.

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