Correlation of Arterial Blood Gas (ABG) and Venous Blood Gas (VBG) in the Undifferentiated Critically Ill Patient

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Christiana Care Health Services
ClinicalTrials.gov Identifier:
NCT01287884
First received: January 31, 2011
Last updated: November 7, 2012
Last verified: November 2012

January 31, 2011
November 7, 2012
October 2010
June 2012   (final data collection date for primary outcome measure)
Degree to which pH and pCO2 correlate between ABG and VBG [ Time Frame: 5 minutes ] [ Designated as safety issue: No ]
ABG and VBG will be obtained 5 minutes apart and compared
Same as current
Complete list of historical versions of study NCT01287884 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Correlation of Arterial Blood Gas (ABG) and Venous Blood Gas (VBG) in the Undifferentiated Critically Ill Patient
Correlation of Arterial Blood Gas (ABG) and Venous Blood Gas (VBG) in the Undifferentiated Critically Ill Patient

The primary objective of this study is to identify a correlation between the pH and pCO2 in arterial and venous blood. The secondary objectives include a correlation of pulse oximetry and arterial pO2 along with subgroup analyses of specific patient populations such as congestive heart failure, chronic obstructive pulmonary disease, diabetic ketoacidosis, pneumonia, overdose, and trauma.

Not Provided
Interventional
Not Provided
Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Patients Needing Blood Gases
Other: Venous Blood Gas
patients who have been identified by the treating physician as needing an ABG will receive an VBG is they consent to take part in the study
No Intervention: Venous Blood Gas
All subjects have an ABG and VBG drawn. No intervention.
Intervention: Other: Venous Blood Gas
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
156
June 2012
June 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age 18 years or older Signed consent Patient in the ED or ICU Have a disease state that necessitates obtaining an ABG Have a disease state that necessitates pulse oximetry monitoring

Exclusion Criteria:

  • Any contraindication to arterial or venous blood draw Prior enrollment in the study during the current hospitalization Pregnancy Prisoners
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01287884
600824
No
Christiana Care Health Services
Christiana Care Health Services
Not Provided
Principal Investigator: Eli Zeserson, MD Christiana Care Health Services
Christiana Care Health Services
November 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP