Agreement Between Venous and Arterial Blood Gas Measurements in the Intensive Care Unit (AVANTI)
This study has been completed.
Sponsor:
University of California, Los Angeles
Collaborator:
Olive View-UCLA Medical Center
Information provided by:
University of California, Los Angeles
ClinicalTrials.gov Identifier:
NCT00569634
First received: December 6, 2007
Last updated: December 2, 2008
Last verified: December 2008
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Purpose
The purpose of this study is to examine the agreement between venous blood gas and arterial blood gas measurements in patients in the Intensive Care Unit.
| Condition | Intervention |
|---|---|
|
Acid-Base Balance |
Procedure: Venous blood gas analysis |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Diagnostic |
| Official Title: | Agreement Between Venous and Arterial Blood Gas Measurements in the Intensive Care Unit |
Resource links provided by NLM:
Further study details as provided by University of California, Los Angeles:
Primary Outcome Measures:
- Agreement between venous and arterial blood gas measurements of pH, pCO2 and bicarbonate [ Time Frame: Duration of Intensive Care Unit Admission ] [ Designated as safety issue: No ]
| Enrollment: | 40 |
| Study Start Date: | January 2008 |
| Study Completion Date: | July 2008 |
| Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| 1 |
Procedure: Venous blood gas analysis
When an ABG is deemed to be necessary as part of ICU management, a central venous sample will also be obtained with minimum delay (always < 2 minutes) between the samples. The samples will be analyzed by a blood gas analyzer as quickly as possible.
|
Detailed Description:
Venous blood gas analysis may be an alternative to arterial blood gas analysis for acid-base status, reducing the need for frequent invasive arterial sampling. The objective of this study is to examine the agreement between ABG and VBG samples for all commonly used parameters (pH, pCO2 and bicarbonate) in a pathologically diverse ICU patient population, specifically analyzing multiple paired arterial and venous samples from each patient.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Adult patients 18 years or older
- Admitted to the Intensive Care Unit (ICU)
- Determined by their treating clinicians to require both a central venous line and arterial line
Exclusion Criteria:
- None
Contacts and Locations
More Information
Publications:
| Responsible Party: | Richard Treger, M.D., Olive View-UCLA Medical Center |
| ClinicalTrials.gov Identifier: | NCT00569634 History of Changes |
| Other Study ID Numbers: | 07H-821001 |
| Study First Received: | December 6, 2007 |
| Last Updated: | December 2, 2008 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of California, Los Angeles:
|
Venous blood gas Arterial blood gas pH pCO2 Bicarbonate |
ClinicalTrials.gov processed this record on May 16, 2013