Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01305564 · ClinicalTrials.gov registry record · NA

A Prospective, Multi-Center Study of the Bard® Denali™ Retrievable Inferior Vena Cava Filter System

A NA study, sponsored by C. R. Bard.

Completed
Registry status
NA
Development phase
200
Enrollment target

NCT01305564: Completed NA study, sponsored by C. R. Bard.

NCT01305564 is a NA study that has completed, run by C. R. Bard. The registered enrollment target is 200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01305564, a NA study, has completed, sponsored by C. R. Bard.

COMPLETED
Registry status
NA
Development phase
200 participants
Enrollment target

Study Summary

The Bard® Denali™ Retrievable Inferior Vena Cava (IVC) study is a prospective, multi-center study which is intended to provide evidence of safety of the placement and retrieval of the Bard® Denali™ Retrievable Inferior Vena Cava Filter in subjects requiring IVC interruption to protect against pulmonary embolism (PE).

Primary Outcome

Technical success of filter placement is defined as the deployment of the filter such that the physician judges the location to be suitable to provide sufficient mechanical protection against Pulmonary Embolism.

Interventions

  • DEVICE Denali inferior vena cava filter

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2011-06
Est. Completion 2015-07
Phase NA
C. R. Bard

75 total trials

What the finished NCT01305564 record still lists

NCT01305564 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 1 intervention - of which Denali inferior vena cava filter is the first listed.

NCT01305564 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01305564 about?

NCT01305564 is a clinical study titled "A Prospective, Multi-Center Study of the Bard® Denali™ Retrievable Inferior Vena Cava Filter System". The Bard® Denali™ Retrievable Inferior Vena Cava (IVC) study is a prospective, multi-center study which is intended to provide evidence of safety of the placement and retrieval of the Bard® Denali™ Retrievable Inferior Vena Cava Filter in subjects requiring IVC interruption to protect against pulmon...

What is the current status of trial NCT01305564?

This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2011-06. Estimated completion is 2015-07.

What interventions are being tested in trial NCT01305564?

The interventions under investigation include: Denali inferior vena cava filter (DEVICE).

Who is sponsoring clinical trial NCT01305564?

This trial is sponsored by C. R. Bard, which has 75 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01305564's enrollment target sits among peer trials

200 506th of 2000 higher than 1,434 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00107289 · 200 participants · Phase 2

    Iodine I 131 Metaiodobenzylguanidine in Treating Patients With Recurrent, Progressive, or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma

  • NCT00109174 · 200 participants · NA

    MRS Measurement of Glutamate and GABA Metabolism in Brain

  • NCT00177268 · 200 participants

    Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research

  • NCT00493688 · 200 participants

    A Study to Determine Whether Perioperative Energy Dynamics Correlates With Postoperative Outcomes

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01305564, the US trial registry maintained by the National Library of Medicine. NCT01305564 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.