Glycosaminoglycans During Septic Shock - a Temporal Study
NCT ID: NCT00814112
Last Updated: 2024-03-15
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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WITHDRAWN
OBSERVATIONAL
2008-11-30
2010-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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1 septic shock
septic shock, ICU
No interventions assigned to this group
2 controls
matched controls
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Clinical sepsis is suspected
* Informed consent from relative
* Study subject must be over 18 years old
Exclusion Criteria
* \>24h post sepsis diagnosis
* Ongoing oral or intravenous cortisone treatment for more than one month.
* Malignancy with metastasis
18 Years
100 Years
ALL
Yes
Sponsors
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Region Skane
OTHER
Responsible Party
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Principal Investigators
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Mikael Bodelsson, professor
Role: PRINCIPAL_INVESTIGATOR
Intensive Care Unit, Lund University Hospital, Sweden
Locations
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Intensive Care Unit, Lund University Hospital
Lund, , Sweden
Countries
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Other Identifiers
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GAGS 293/2008
Identifier Type: -
Identifier Source: org_study_id
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