NCT00303043

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2006

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2006

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

March 14, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 15, 2006

Completed
3.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2009

Completed
Last Updated

December 30, 2009

Status Verified

March 1, 2009

Enrollment Period

3.3 years

First QC Date

March 14, 2006

Last Update Submit

December 29, 2009

Conditions

Critically Ill

Keywords

Hemodynamic monitoringMixed venous saturationCritically ill patients

Study Arms (1)

1

Procedure: Mixed venous saturation monitoring

Interventions

Mixed venous saturation monitoringPROCEDURE

Mixed venous saturation monitoring

1

Eligibility Criteria

Age16 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Critically ill patients with a central venous catheter

You may qualify if:

  • Critically ill patients with a central venous catheter

You may not qualify if:

  • Patients with pulmonary catheter

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena

Milan, mi, 20145, Italy

Location

MeSH Terms

Conditions

Critical Illness

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Davide Chiumello, MD

    Fondazione Ospedale Maggiore Policlinico Mangiagalli Regina Elena

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 14, 2006

First Posted

March 15, 2006

Study Start

March 1, 2006

Primary Completion

July 1, 2009

Study Completion

July 1, 2009

Last Updated

December 30, 2009

Record last verified: 2009-03

Locations

IT(1)