Procalcitonin as a Marker for the Length of Antibiotic Treatment in Peritonitis and Intra-abdominal Infections
NCT ID: NCT01155739
Last Updated: 2014-12-19
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
162 participants
OBSERVATIONAL
2009-06-30
2014-06-30
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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procalcitonine monitoring
PCT group: antibiotic use is tailored by serum procalcitonin values, determined every 48houres.
No interventions assigned to this group
control group
control group: antibiotic use and length of treatment as defined by guidelines
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patient requiring surgery for peritonitis or intra-abdominal infection following: perforation, necrosis, previous operation...
* Mannheim Peritonitis score \> 14
* SIRS present
* Probability of survival \> 72h
* Informed consent by patient/relatives
Exclusion Criteria
* Long date corticoid treatment
* Immunosuppression
* Thyroid medullary carcinoma
* Anaphylactic shock
* Acute hepatic deficiency
18 Years
ALL
No
Sponsors
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University of Lausanne Hospitals
OTHER
Responsible Party
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Nicolas DEMARTINES
professor of surgery
Principal Investigators
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Steve Aellen, MD
Role: PRINCIPAL_INVESTIGATOR
Department of visceral surgery, university hospital
Locations
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University Hospital of Lausanne
Lausanne, , Switzerland
Countries
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Other Identifiers
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141/08, Propéritonite
Identifier Type: -
Identifier Source: org_study_id