We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Hemodynamic Monitoring With Mixed Venous Saturation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00303043
First Posted: March 15, 2006
Last Update Posted: December 30, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Policlinico Hospital
  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

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

Enrollment: 30
Study Start Date: March 2006
Study Completion Date: July 2009
Primary Completion Date: July 2009 (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

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   16 Years to 80 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00303043


Locations
Italy
Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena
Milano, MI, Italy, 20145
Sponsors and Collaborators
Policlinico Hospital
Investigators
Principal Investigator: Davide Chiumello, MD Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena
  More Information

Responsible Party: Davide Chiumello, Policlinico Hospital
ClinicalTrials.gov Identifier: NCT00303043     History of Changes
Other Study ID Numbers: 2000
First Submitted: March 14, 2006
First Posted: March 15, 2006
Last Update Posted: December 30, 2009
Last Verified: March 2009

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

Additional relevant MeSH terms:
Critical Illness
Disease Attributes
Pathologic Processes