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Hemodynamic Monitoring With Mixed Venous Saturation
This study is currently recruiting participants.
Verified by Policlinico Hospital, October 2008
Sponsored by: Policlinico Hospital
Information provided by: Policlinico Hospital
ClinicalTrials.gov Identifier: NCT00303043
  Purpose

In this study the investigators aim to evaluate the utility of a continuous mixed venous saturation monitoring compared to a clinical examination in a group of critically ill patients.


Condition Intervention
Critically Ill
Procedure: Mixed venous saturation monitoring

U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: Hemodynamic Monitoring. The Continuous Measurement of Mixed Venous Saturation Compared to Clinical Valuation: A Pilot Study

Further study details as provided by Policlinico Hospital:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 30
Study Start Date: March 2006
Estimated Study Completion Date: December 2008
Estimated Primary Completion Date: December 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
1 Procedure: Mixed venous saturation monitoring
Mixed venous saturation monitoring

Detailed Description:

We will compare possible difference in terms of sensibility and specificity regarding the continuous mixed venous saturation monitoring compared to clinical examination in a group of critically ill patients.

  Eligibility

Ages Eligible for Study:   16 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Critically ill patients with a central venous catheter

Criteria

Inclusion Criteria:

  • Critically ill patients with a central venous catheter

Exclusion criteria:

  • Patients with pulmonary catheter
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00303043

Contacts
Contact: Davide Chiumello, MD 39-025-503-3237 chiumello@libero.it

Locations
Italy, Mi
Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena Recruiting
Milano, Mi, Italy, 20145
Contact: Davide Chiumello, MD     39-025-503-3237     chiumello@libero.it    
Principal Investigator: Davide Chiumello, MD            
Sponsors and Collaborators
Policlinico Hospital
Investigators
Principal Investigator: Davide Chiumello, MD Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena
  More Information

Responsible Party: Policlinico Hospital ( Davide Chiumello )
Study ID Numbers: 2000
Study First Received: March 14, 2006
Last Updated: October 22, 2008
ClinicalTrials.gov Identifier: NCT00303043  
Health Authority: Italy: Ministry of Health

Keywords provided by Policlinico Hospital:
Hemodynamic monitoring
Mixed venous saturation
Critically ill patients

Study placed in the following topic categories:
Critical Illness

Additional relevant MeSH terms:
Disease Attributes
Pathologic Processes

ClinicalTrials.gov processed this record on January 16, 2009