NCT00596921

Brief Summary

This study proposes to examine the correlation of central venous pressure to measures of the diameter of the inferior vena cava as determined by bedside ultrasonography.

Trial Health

50
Monitor

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Status
unknown

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 8, 2008

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 17, 2008

Completed
Last Updated

January 17, 2008

Status Verified

January 1, 2008

First QC Date

January 8, 2008

Last Update Submit

January 16, 2008

Conditions

Keywords

UltrasonographyCentral Venous PressureNoninvasive monitoringShockResuscitation

Outcome Measures

Primary Outcomes (1)

  • Bedside ultrasound measurement of the diameter of the inferior vena cava and simultaneously measured central venous pressure.

    Cross-sectional

Secondary Outcomes (1)

  • Anatomic view and phase of respiration at the time of measurements.

    Cross-sectional

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Hospitalized patients with central venous monitoring in place.

You may qualify if:

  • CVP or right heart catheter that is already in place and functioning properly

You may not qualify if:

  • Supine position or placement of ultrasound probe on abdomen is contraindicated.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

ShockHypovolemiaEdema

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Officials

  • Robert A De Lorenzo, MD

    Brooke Army Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Robert A De Lorenzo, MD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
FED

Study Record Dates

First Submitted

January 8, 2008

First Posted

January 17, 2008

Last Updated

January 17, 2008

Record last verified: 2008-01