Quality Control of Ventral Hernia Surgery by Prospective Registration
NCT ID: NCT04624100
Last Updated: 2023-11-28
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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NOT_YET_RECRUITING
5000 participants
OBSERVATIONAL
2024-07-01
2026-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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All consecutive patients with primary ventral or incisional hernia
Hernia repair
Primary or mesh repair of primary ventral or incisional hernia
Interventions
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Hernia repair
Primary or mesh repair of primary ventral or incisional hernia
Eligibility Criteria
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Inclusion Criteria
* Male and female
* 18 years or older
* Operated of supervised by a participating surgeon (participating in this study is not necessarily by a whole surgical department of one of the 18 participating Belgian hospitals, but by specific surgeons)
* Elective and emergency surgery
* Signed informed consent form
Exclusion Criteria
* Not operated or supervised by participating surgeon
* Pregnant at inclusion in the registry
* No signed informed consent form
18 Years
ALL
No
Sponsors
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Belgian Section for Abdominal Wall Surgery, section of the Royal Belgian Society for Surgery
UNKNOWN
Universitaire Ziekenhuizen KU Leuven
OTHER
Responsible Party
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Marc Miserez
MD PhD
Other Identifiers
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S62600
Identifier Type: -
Identifier Source: org_study_id