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Agreement Between Arterial, Central Venous, and Peripheral Venous Lactate Measurements in the Intensive Care Unit

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01408251
First Posted: August 3, 2011
Last Update Posted: August 3, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Olive View-UCLA Education & Research Institute
  Purpose
The purpose of this study is to see if blood obtained from a vein (smaller blood vessel) can be used instead of blood obtained from an artery (larger blood vessel).

Condition
Acid-base Analysis

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Agreement Between Arterial, Central Venous, and Peripheral Venous Lactate in the Intensive Care Unit

Further study details as provided by Olive View-UCLA Education & Research Institute:

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)
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Intensive Care Unit patients requiring both an arterial line and central venous line as part of their clinical care
Criteria

Inclusion Criteria:

  • Patients admitted to the ICU and requiring both an arterial line and central venous line as prt of their clinical care

Exclusion Criteria:

  • Patient did not desire to participate
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01408251


Sponsors and Collaborators
Olive View-UCLA Education & Research Institute
Investigators
Principal Investigator: Richard M Treger, M.D. VA Greater Los Angeles Healthcare System
  More Information

Responsible Party: Richard Treger/Principal Investigator, VA Greater Los Angeles Healthcare System
ClinicalTrials.gov Identifier: NCT01408251     History of Changes
Other Study ID Numbers: 193070
First Submitted: August 1, 2011
First Posted: August 3, 2011
Last Update Posted: August 3, 2011
Last Verified: August 2011