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Hemodynamic Monitoring With Mixed Venous Saturation

This study has been completed.
Sponsor:
Information provided by:
Policlinico Hospital
ClinicalTrials.gov Identifier:
NCT00303043
First received: March 14, 2006
Last updated: December 29, 2009
Last verified: March 2009
  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

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
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: 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

No publications provided

Responsible Party: Davide Chiumello, Policlinico Hospital
ClinicalTrials.gov Identifier: NCT00303043     History of Changes
Other Study ID Numbers: 2000
Study First Received: March 14, 2006
Last Updated: December 29, 2009
Health Authority: Italy: Ministry of Health

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

Additional relevant MeSH terms:
Critical Illness
Disease Attributes
Pathologic Processes

ClinicalTrials.gov processed this record on November 24, 2014