Substudy - Evaluation of Patients With Iliac Vein Thrombosis
NCT ID: NCT03148548
Last Updated: 2019-10-28
Study Results
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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COMPLETED
85 participants
OBSERVATIONAL
2016-11-30
2018-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
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
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
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;
Eligibility Criteria
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Inclusion Criteria
* subjects with iliofermoral thrombosis, which has been proven by objective measurements (Duplex sonography, phlebography, CT/MRT) later than 1996
Exclusion Criteria
* \> 80 years
* surface or deep vein thrombosis without affection of pelvis
18 Years
80 Years
ALL
No
Sponsors
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Cardioangiologisches Centrum Bethanien
OTHER
Responsible Party
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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
Countries
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Other Identifiers
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ILIACA-PTS
Identifier Type: -
Identifier Source: org_study_id
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