Analysis of Sublingual Glycocalyx Damage at ICU Admission to Predict Risk of Death
NCT ID: NCT03847493
Last Updated: 2022-11-07
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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UNKNOWN
100 participants
OBSERVATIONAL
2019-04-15
2023-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with suspected sepsis
Patients admitted in the ICU with the clinical suspicion of infection/sepsis.
Endothelial Glycocalyx
Non-invasive assessment of endothelial glycocalyx dimensions.
Non-sepsis Patients (control group)
Patients admitted in the ICU with other conditions apart from infection/sepsis.
Endothelial Glycocalyx
Non-invasive assessment of endothelial glycocalyx dimensions.
Interventions
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Endothelial Glycocalyx
Non-invasive assessment of endothelial glycocalyx dimensions.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital Muenster
OTHER
Responsible Party
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Principal Investigators
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Philipp Kümpers, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital Muenster
Locations
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Universitiy Hospital Muenster
Münster, , Germany
Countries
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Other Identifiers
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ASGARD
Identifier Type: -
Identifier Source: org_study_id
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