Procalcitonin in Pleural Pleuritis

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Universitaire, Amiens
ClinicalTrials.gov Identifier:
NCT01011881
First received: November 10, 2009
Last updated: June 8, 2016
Last verified: June 2016

November 10, 2009
June 8, 2016
October 2009
February 2011   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT01011881 on ClinicalTrials.gov Archive Site
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Procalcitonin in Pleural Pleuritis
Evaluation de la Mesure du Taux de la Procalcitonine Dans Les Liquides Pleuraux
The purpose of this study is to determine pleural level of procalcitonin in differents situations of pleuritis.

Determine pleural level of procalcitonin in pleuritis. Two periods First period evaluation in vitro study/ Determine adequat technique included type of samples tubes for adequat analysis.

Second periods : Patient with pleuritis . Empyema or not

Observational
Observational Model: Cohort
Time Perspective: Prospective
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Non-Probability Sample
patients with pleuritis
  • Pleuritis
  • Pleural Empyema
Other: pleural level of procalcitonin
no intervention
patients with pleuritis
Intervention: Other: pleural level of procalcitonin
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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
34
February 2011
February 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Pleuritis
  • Hospitalisation

Exclusion Criteria:

Both
18 Years to 99 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01011881
PI09-DR-DOUADI
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Centre Hospitalier Universitaire, Amiens
Centre Hospitalier Universitaire, Amiens
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Centre Hospitalier Universitaire, Amiens
June 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP