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IL 6 Measurement Using a New Densitometric Bedside (POC) Test

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00525369
First Posted: September 5, 2007
Last Update Posted: September 5, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Charite University, Berlin, Germany
September 4, 2007
September 5, 2007
September 5, 2007
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No Changes Posted
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IL 6 Measurement Using a New Densitometric Bedside (POC) Test
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In a equivalence analysis, we determined whether IL-6 can be assessed using a new densitometric point-of-care (POC) assay (turn-around -time: 20 minutes).IL-6 measurements were compared to test results obtained with conventional ELISA analysis
In an equivalence analysis, we determined whether IL-6 can be assessed using a new densitometric point-of-care (POC) assay (turn-around -time: 20 minutes) that allows IL-6 measurements at the bedside. We then compared the respective test results to those obtained with conventional ELISA analysis
Observational
Observational Model: Defined Population
Time Perspective: Cross-Sectional
Time Perspective: Prospective
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Sepsis, Septic Shock
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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Inclusion Criteria:

  • Age 18-90
  • Written informed consent
Sexes Eligible for Study: All
18 Years to 90 Years   (Adult, Senior)
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Contact information is only displayed when the study is recruiting subjects
Germany
 
 
NCT00525369
STU-IL-6-1
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Charite University, Berlin, Germany
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Principal Investigator: Hans-Georg Schlosser, MD Charite University, Berlin, Germany
Principal Investigator: Joerg C Schefold, MD Charite University, Berlin, Germany
Charite University, Berlin, Germany
September 2007