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CompletedNCT05785676CONFIALUpdated Apr 9, 2026

ALN OATF Vena Cava Filter

An observational study in Pulmonary Embolism, sponsored by Assistance Publique - Hôpitaux de Paris. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-09.

Sponsored by Assistance Publique - Hôpitaux de Paris · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Migration of a thrombus in the pulmonary circulation is the leading cause of pulmonary embolism (PE). It can be prevented mechanically by implanting a vena cava filter (VCF) in the inferior vena cava. The implation of a VCF is indicated for patients with acute PE and a contraindication to anticoagulation, with an acute deep vein thrombosis (DVT) without PE and a contraindication to anticoagulation or with acute venous thromboembolism (less than 3 months) in whom an interventional gesture at hemorrhagic and thromboembolic risk contraindicates anticoagulation.

The purpose of this study is to describe the rates of implantation, removal and complications associated with the use of the optional ALN OATF VCF in current practice.

02

Conditions studied

  • Pulmonary Embolism

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Keywords

  • Vena Cava Filter
03

In context

Pulmonary Embolism

739 studies on the registry are indexed under Pulmonary Embolism; 159 are open to participants now.

This study's enrollment of 50 is below the median of 392 across 324 observational studies indexed under Pulmonary Embolism.

Browse Pulmonary Embolism studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,505 studies on the registry; 1,006 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adult patients requiring a vena cave filter

Inclusion criteria

  • Patient implanted with an ALN OATF VCF
  • Patient informed

Exclusion criteria

Exclusion Criteria:

  • Minor patient
  • Adult patient under a legal protection measure
  • Pregnant, parturient or breastfeeding women
  • Patient who refused to participate
  • Patient who cannot or does not wish to be followed by the Interventional Radiology Department
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (actual)
Patient registry
No

Groups and cohorts

  • Vena Cava Filter

    Participants implanted with the vena cava filter OATF (ALN)

    Device: Filter implantation

Interventions

  • DeviceFilter implantation

    Implantation of OATF ALN vena cava filter

06

What researchers measure

Primary outcomes

  1. Filter implantation

    Rate of technical success of filter implantation

    Time frame: day 0

Secondary outcomes

  1. Filter removal

    Rate of filter removal

    Time frame: up to 1 year

07

Study locations

1 site
  • AP-HP - Hôpital Européen Georges-Pompidou Paris, France
    Paris, Île-de-France Region 75908, France
08

References and documents

Individual participant data

Plan to share: Yes — Individual participant data (IPD) that underlie results in publication could be shared. IPD detailed in the protocol of a planned metaanalysis could be shared

Supporting information: Study protocol, Icf

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05785676
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Aln2b SARL
Responsible party
Sponsor
First posted
Mar 27, 2023
Start date
Feb 14, 2023
Primary completion
Jul 31, 2024
Completion
Jul 31, 2025
Last update
Apr 9, 2026

Study contacts

Olivier PELLERIN, MD - PhD
principal investigator · Assistance Publique - Hôpitaux de Paris

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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