Bedside Ultrasound Measurement of the Inferior Vena Cava Correlates to Central Venous Pressure
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Purpose
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.
| Condition |
|---|
|
Shock Hypovolemia Hypervolemia |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Cross-Sectional |
| Official Title: | Bedside Ultrasound Measurement of the Inferior Vena Cava Correlates to Central Venous Pressure |
- Bedside ultrasound measurement of the diameter of the inferior vena cava and simultaneously measured central venous pressure. [ Time Frame: Cross-sectional ] [ Designated as safety issue: No ]
- Anatomic view and phase of respiration at the time of measurements. [ Time Frame: Cross-sectional ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 100 |
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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Hospitalized patients with central venous monitoring in place.
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.
Contacts and Locations
More Information
No publications provided
| Responsible Party: | COL Robert De Lorenzo, Brooke Army Medical Center |
| ClinicalTrials.gov Identifier: | NCT00596921 History of Changes |
| Other Study ID Numbers: | C.2008.029, CIRO.2008111 |
| Study First Received: | January 8, 2008 |
| Last Updated: | January 16, 2008 |
| Health Authority: | United States: Federal Government |
Keywords provided by Brooke Army Medical Center:
|
Ultrasonography Central Venous Pressure Noninvasive monitoring Shock Resuscitation |
Additional relevant MeSH terms:
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Shock Hypovolemia Pathologic Processes |
ClinicalTrials.gov processed this record on May 16, 2013