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A Simple Clinical Tool to Help Assess Patient Volume (Fluid) Status

NCT00599794 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 84

Last updated 2008-01-24

No results posted yet for this study

Summary

Patients may have actual or relative intravascular volume depletion in a number of different disease states, particularly with sepsis syndrome. However, it is clinically difficult to determine volume status without invasive monitoring, which may cause unintended complications. Our hypothesis is that we can accurately estimate central venous pressure, which is a surrogate marker of volume status, with a noninvasive portable ultrasound device.

Conditions

Sponsors & Collaborators

  • Allina Health System

    collaborator OTHER

  • Mayo Clinic

    lead OTHER

Principal Investigators

  • A. S. Keller, MD · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2007-10-31
Completion
2008-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00599794 on ClinicalTrials.gov