Venous Thrombo-Embolism Imaging Database (VTE-ID)

NCT ID: NCT06258694

Last Updated: 2024-02-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

2208 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-01-14

Study Completion Date

2021-02-15

Brief Summary

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The purpose of this study is to identify and validate new imaging biomarkers allowing an individual phenotyping of patient with venous thrombo-embolism (VTE), mainly in terms of recurrence risk assessment and to distinguish provoked from unprovoked VTE. To do so, the investigators will create a retrospective imaging database including multiple imaging modalities, performed at diagnosis of the VTE.

Detailed Description

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Using a large imaging data in VTE (including ultrasound, CT-scan and Ventilation/Perfusion lung scan), the investigators will search for association between imaging data and VTE phenotypes, mainly in terms of recurrence risk assessment and to distinguish provoked from unprovoked VTE. Then, using a radiomic approach, the investigators will try to identify new imaging biomarkers able to provide an individual phenotyping in these patients.

These imaging biomarkers will be validated using an internal cross validation technique.

Conditions

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Venous Thromboembolism Deep Vein Thrombosis Pulmonary Embolism

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* 18 years or older.
* Confirmed VTE diagnosis (deep vein thrombosis or pulmonary embolism).
* Inclusion in the EDITH (Etude des Déterminants et Interaction de la THrombose veineuse) between November 2009 and November 2019.
* No opposition to be included in the present study.

Exclusion Criteria

* Patients under 18 years old.
* Patients under judicial protection.
* Patient physically or cognitively unable to give consent.
* Refusal to participate.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Brest University Hospital

Brest, Finistere, France

Site Status

Countries

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France

Other Identifiers

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29BRC20.0326 - VTE-ID

Identifier Type: -

Identifier Source: org_study_id

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