- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00596921
Bedside Ultrasound Measurement of the Inferior Vena Cava Correlates to Central Venous Pressure
January 16, 2008 updated by: Brooke Army Medical Center
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.
Study Overview
Status
Unknown
Conditions
Detailed Description
Central venous pressure (CVP) is a key physiologic estimate of preload, which in turn helps define the vascular fluid status.
It is a particularly important parameter to measure in critically ill and injured patients who may require resuscitation.
Unfortunately, measurement of the CVP requires invasive central venous catheters which can be difficult or time-consuming to insert.
A non-invasive means of inferring the CVP would provide clinicians with an alternative.
Preliminary data suggests that the diameter of the vena cava may reflect the CVP.
Ultrasonography can provide reliable measures of internal body structures including the vena cava, and therefore may be useful in this regard.
Collecting simultaneous values of vena cava diameter and CVPs will allow for the identification and quantification of correlation.
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Robert A De Lorenzo, MD
- Phone Number: 210.916.0607
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Hospitalized patients with central venous monitoring in place.
Description
Inclusion Criteria:
- CVP or right heart catheter that is already in place and functioning properly
Exclusion Criteria:
- Supine position or placement of ultrasound probe on abdomen is contraindicated.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Bedside ultrasound measurement of the diameter of the inferior vena cava and simultaneously measured central venous pressure.
Time Frame: Cross-sectional
|
Cross-sectional
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Anatomic view and phase of respiration at the time of measurements.
Time Frame: Cross-sectional
|
Cross-sectional
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Robert A De Lorenzo, MD, Brooke Army Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
January 8, 2008
First Submitted That Met QC Criteria
January 16, 2008
First Posted (ESTIMATE)
January 17, 2008
Study Record Updates
Last Update Posted (ESTIMATE)
January 17, 2008
Last Update Submitted That Met QC Criteria
January 16, 2008
Last Verified
January 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- C.2008.029
- CIRO.2008111
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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