Substudy - Evaluation of Patients With Iliac Vein Thrombosis

NCT ID: NCT03148548

Last Updated: 2019-10-28

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

85 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-11-30

Study Completion Date

2018-01-31

Brief Summary

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Patients with previous diagnosis of iliac vein thrombosis are enrolled in this registry. Using standardized questionnaire, clinical data detailing venous thromboembolism and contributing VTE risk factors are recorded. Results of technical and laboratory investigations including screening of thrombophilic disorders were additionally entered into the database.

Detailed Description

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Conditions

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Iliac Vein Thrombosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Patients with iliofermoral thrombosis without rekanalisation

subjects with proven iliofemoral thrombosis (V. cava-aplasia, pelvic vein thrombosis, VTE) which was proven by objective methods such as Duplex sonography, CT/MRT, phlebography and who did not undergo recanalisation

thrombophilia screening

Intervention Type GENETIC

genetic Evaluation of Factor-V-Leiden, Factor-II\_G20210A Mutation;

Patients with ilifermoral thrombosis with rekanalisation

subjects with proven iliofemoral thrombosis (V. cava-aplasia, pelvic vein thrombosis, VTE) which was proven by objective methods such as Duplex sonography, CT/MRT, phlebography and who did undergo recanalisation

thrombophilia screening

Intervention Type GENETIC

genetic Evaluation of Factor-V-Leiden, Factor-II\_G20210A Mutation;

Interventions

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thrombophilia screening

genetic Evaluation of Factor-V-Leiden, Factor-II\_G20210A Mutation;

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* \>18 years
* subjects with iliofermoral thrombosis, which has been proven by objective measurements (Duplex sonography, phlebography, CT/MRT) later than 1996

Exclusion Criteria

* \<18 years
* \> 80 years
* surface or deep vein thrombosis without affection of pelvis
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cardioangiologisches Centrum Bethanien

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Edelgard Lindhoff-Last, Prof.

Role: PRINCIPAL_INVESTIGATOR

Cardioangiologisches Centrum Bethanien

Locations

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Cardioangiologisches Centrum Bethanien

Frankfurt am Main, Hesse, Germany

Site Status

Countries

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Germany

Other Identifiers

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ILIACA-PTS

Identifier Type: -

Identifier Source: org_study_id

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