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Trial · NCT04066764

Rivaroxaban and Vitamin K Antagonists for the Anticoagulation for the Implantation of Vena Cava Filters

NCT04066764, Phase 3, Unknown, Second Affiliated Hospital, Zhejiang University, School of Medicine

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Rivaroxaban and Vitamin K Antagonists for the Anticoagulation for the Implantation of Vena Cava Filters. Trials, record NCT04066764. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04066764

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Rivaroxaban and Vitamin K Antagonists for the Anticoagulation for the Implantation of Vena Cava Filters
NCT number
NCT04066764
Status
Unknown
Phases
Phase 3
Enrollment
200 participants, estimated
Lead sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
Conditions
Venous Thromboembolism
Interventions
Rivaroxaban, Warfarin, Nadroparin
First posted
2019-08-26
Last updated
2024-04-18

Source ClinicalTrials.gov

Registered outcomes7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryAll cause mortality4 months after the filter is retrievedPercentage of participants with all deaths
PrimaryPulmonary embolism related mortality4 months after the filter is retrieved
PrimaryPercentage of Participants with bleeding4 months after the filter is retrievedClinically relevant bleeding is defined as a composite of major or clinically relevant nonmajor bleeding
PrimaryPercentage of Participants With Symptomatic Recurrent Venous Thromboembolism4 months after the filter is retrievedthe Composite of Recurrent Deep Vein Thrombosis \[DVT\] or Fatal or Non-fatal Pulmonary Embolism \[PE\]
SecondaryPercentage of Participants With IVC Filter Retrieval Failure4 months after the filter is retrieved
IVC filter retrieval failure is relevant to IVC filter complications (e.g. IVC thrombosis, IVC perforation, IVC filter migration or tilting and IVC filter embolization), system factors and technical factors.
SecondaryPercentage of Participants With an Event for Net Clinical Benefit4 months after the filter is retrievedcomposite of primary efficacy outcomes and major bleeding, assessed in the intention-to-treat population.
SecondaryPercentage of Participants With Other Vascular Events4 months after the filter is retrieved
All pre-defined vascular events (ST segment elevation myocardial infarction, non ST segment elevation myocardial infarction, acute coronary syndrome, unstable angina, ischemic stroke, transient ischemic attack, pulmonary embolism, non-central nervous system systemic embolism or vascular death) will be assessed based results/films/images of confirmatory testing, and/or case summaries.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers10

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
11228276BACKGROUNDPubMed
18579812BACKGROUNDPubMed
19411100BACKGROUNDPubMed
21128814BACKGROUNDPubMed
22449293BACKGROUNDPubMed
25851122BACKGROUNDPubMed
26867832BACKGROUNDPubMed
27030066BACKGROUNDPubMed
28510665BACKGROUNDPubMed
34697109DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04066764

GET https://conductscience.org/api/trials/v1/NCT04066764/registered