Metabolomic in Critical Ill Patients

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by:
Università Vita-Salute San Raffaele
ClinicalTrials.gov Identifier:
NCT01506674
First received: January 9, 2012
Last updated: April 4, 2014
Last verified: April 2014

January 9, 2012
April 4, 2014
January 2012
December 2015   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT01506674 on ClinicalTrials.gov Archive Site
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Metabolomic in Critical Ill Patients
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Analysis of blood, urinary, and intrathecal metabolites of critical ill patients will be checked for possible correlations between metabolomics patterns and patients' outcomes.

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Observational
Observational Model: Cohort
Time Perspective: Prospective
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Non-Probability Sample

Critical ill patients

Metabolomic
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criticall ill patients
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
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December 2015
December 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • patients with severe left or right ventricular dysfunction undergoing cardiac surgery
  • patients undergoing ablation of ventricular tachycardia
  • patients with febrile neutropenia after chemotherapy or allogeneic transplant for haematological diseases

Exclusion Criteria:

  • pregnant women
  • no written consent
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Italy
 
NCT01506674
HSR CEmet
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Università Vita-Salute San Raffaele
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Università Vita-Salute San Raffaele
April 2014

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