Last reviewed · How we verify
NCT02161965: VICTORIA
Vascular CalcIfiCation and sTiffness Induced by ORal antIcoAgulation
Phase 4 trial testing Rivaroxaban in Permanent Atrial Fibrillation in 51 participants. Completed in 16 February 2018.
31 December 2016
Quick facts
| Lead sponsor | University Hospital, Angers |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 51 |
| Start date | 21 May 2013 |
| Primary completion | 31 December 2016 |
| Estimated completion | 16 February 2018 |
| Sites | 1 location across France |
Drugs / interventions tested
- Rivaroxaban (rivaroxaban) — full drug profile →
- Fluindione (FLUINDIONE) — full drug profile →
- Warfarin (warfarin) — full drug profile →
Conditions studied
- Permanent Atrial Fibrillation — all drugs for Permanent Atrial Fibrillation →
- Venous Thrombosis — all drugs for Venous Thrombosis →
- Pulmonary Embolism — all drugs for Pulmonary Embolism →
- Anticoagulation Treatment at Least > or = to 12-month — all drugs for Anticoagulation Treatment at Least > or = to 12-month →
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):
-
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:
- PubMed search for NCT02161965
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other University Hospital, Angers trials
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02161965 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University Hospital, Angers
- Last refreshed: 7 November 2019
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.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing