- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01506674
Metabolomic in Critical Ill Patients
January 16, 2024 updated by: Giovanni Landoni, Università Vita-Salute San Raffaele
Analysis of blood, urinary, and intrathecal metabolites of critical ill patients will be checked for possible correlations between metabolomics patterns and patients' outcomes.
Study Overview
Status
Terminated
Conditions
Study Type
Observational
Enrollment (Actual)
94
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Mi
-
Milano, Mi, Italy, 20132
- Università Vita-Salute San Raffaele
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 95 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Critical ill patients
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
criticall ill patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Metabolomic patterns to identify poor outcome
Time Frame: hospital stay (approximately two weeks)
|
hospital stay (approximately two weeks)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 27, 2015
Primary Completion (Actual)
October 31, 2017
Study Completion (Actual)
April 6, 2023
Study Registration Dates
First Submitted
January 9, 2012
First Submitted That Met QC Criteria
January 9, 2012
First Posted (Estimated)
January 10, 2012
Study Record Updates
Last Update Posted (Actual)
January 18, 2024
Last Update Submitted That Met QC Criteria
January 16, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- HSR CEmet
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.