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
  Purpose

Analysis of blood, urinary, and intrathecal metabolites of critical ill patients will be checked for possible correlations between metabolomics patterns and patients' outcomes.


Condition
Metabolomic

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Further study details as provided by Università Vita-Salute San Raffaele:

Study Start Date: January 2012
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts
criticall ill patients

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Critical ill patients

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01506674

Locations
Italy
Università Vita-Salute San Raffaele
Milano, Mi, Italy, 20132
Sponsors and Collaborators
Università Vita-Salute San Raffaele
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT01506674     History of Changes
Other Study ID Numbers: HSR CEmet
Study First Received: January 9, 2012
Last Updated: April 4, 2014
Health Authority: Italy: Ministry of Health

ClinicalTrials.gov processed this record on July 29, 2014