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Metabolomic in Critical Ill Patients

U

Università Vita-Salute San Raffaele

Status

Terminated

Conditions

Metabolomic

Study type

Observational

Funder types

Other

Identifiers

NCT01506674
HSR CEmet

Details and patient eligibility

About

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

Enrollment

94 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

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
  • patients undergoing thoracoabdominal vascular surgery

Exclusion criteria

  • pregnant women
  • no written consent

Trial design

94 participants in 1 patient group

criticall ill patients

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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