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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00303043
Other study ID # 2000
Secondary ID
Status Completed
Phase N/A
First received March 14, 2006
Last updated December 29, 2009
Start date March 2006
Est. completion date July 2009

Study information

Verified date March 2009
Source Policlinico Hospital
Contact n/a
Is FDA regulated No
Health authority Italy: Ministry of Health
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Both
Age group 16 Years to 80 Years
Eligibility Inclusion Criteria:

- Critically ill patients with a central venous catheter

Exclusion criteria:

- Patients with pulmonary catheter

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
Mixed venous saturation monitoring
Mixed venous saturation monitoring

Locations

Country Name City State
Italy Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena Milano MI

Sponsors (1)

Lead Sponsor Collaborator
Policlinico Hospital

Country where clinical trial is conducted

Italy, 

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