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Clinical Trials/NCT00666003
NCT00666003
Completed
Not Applicable

Hemodynamic Assessment Comparison Between Arterial Pressure Cardiac Output Monitor and Crit Line Utilized During Renal Replacement Therapy

Baystate Medical Center1 site in 1 country26 target enrollmentApril 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Renal Failure
Sponsor
Baystate Medical Center
Enrollment
26
Locations
1
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Fluid and volume management are a challenging part of critical care and the difficulties increase in the face of renal failure. Utilizing the Crit-Line to monitor blood volume changes in conjunction with arterial pressure cardiac output monitoring may lead to better understanding of the impact fluid removal during dialysis has on hemodynamics.

Detailed Description

Patients in an ICU often require large amounts of IV fluid to maintain adequate cardiac function. In patients with renal failure, the ability to gauge adequacy of circulating blood volume based on urine output is obviously lacking. The FDA approved devices called Flotrac/Vigileo and Crit-Line are used in this setting to determine adequacy of fluid resuscitation. This study proposes to use the data collected in a retrospective manner to determine if correlation of the various measured parameters can serve as a predictor of hemodynamic status.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
November 2009
Last Updated
15 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Indwelling arterial catheter
  • Require dialysis
  • CVP in place
  • Use of Crit-Line and Flotrak device

Exclusion Criteria

  • Aortic Regurgitation
  • Use of an intra-aortic balloon pump
  • Weight less than 90 lbs
  • Cardiac arrhythmias

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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