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NCT04846725 Clinical Trial

Predictors of Attempted Inferior Vena Cava Filters Retrieval.

Venous Thromboembolic Disease Clinical Trial

Official title:
Predictors of Attempted Inferior Vena Cava Filters Retrieval.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04846725
Other study ID # IRBN372021/CHUSTE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2019
Est. completion date August 1, 2020

Study information
Verified date April 2021
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The InferiorVena Cava (IVC) with filters has been recommended when there is a contraindication or a failure of anticoagulation. Due to the side effects related to the filters, it is recommended to remove them as soon as possible. It's a retrospective study in a French hospital to evaluate the retrieval rate and predictors of filter removal. All the data of consecutive patients who had a retrievable InferiorVena Cava Filter (IVCF) inserted in the investigator center between April 2012 and November 2019 are included.

Recruitment information / eligibility
Status Completed
Enrollment 356
Est. completion date August 1, 2020
Est. primary completion date August 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients who had a cave filter placement at Saint-Etienne Hospital between april 2012 and november 2019. Exclusion Criteria: - None

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Data collection
Collect in medical records : Filter's retrieval rate Complications of vena cava filters Predictive factors of attempted inferior vena cava filters retrieval: age, the distance between the patient's home and the hospital, the indication or not given by the therapeutic medicine department, patients referred by external structures, patients whose filter was installed during the medical on-call period, the absence of a written request for filter placement, the presence of active neoplasia at the time of filter placement, a peri-surgical context.

Locations
Country Name City State
France Chu Saint-Etienne Saint-Étienne

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Filter's retrieval rate (%) Collect in medical records. Month: 2
Secondary Predictive factors of attempted inferior vena cava filters retrieval Collect in medical records. Month: 2
Secondary Adverse event of vena cava filters Collect in medical records. Month: 2
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