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
86 participants
OBSERVATIONAL
2022-01-10
2022-09-14
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Laparotomy
Patients undergoing laparotomy
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patient able to provide informed consent
Exclusion Criteria
* Patients unable to provide informed consent
18 Years
ALL
Yes
Sponsors
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The Cleveland Clinic
OTHER
Responsible Party
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Michael Rosen
Professor of Surgery
Locations
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Cleveland Clinic Main Campus
Cleveland, Ohio, United States
Countries
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Other Identifiers
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21-1036
Identifier Type: -
Identifier Source: org_study_id
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