- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01408251
Agreement Between Arterial, Central Venous, and Peripheral Venous Lactate Measurements in the Intensive Care Unit
August 1, 2011 updated by: Olive View-UCLA Education & Research Institute
Agreement Between Arterial, Central Venous, and Peripheral Venous Lactate in the Intensive Care Unit
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).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
40
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
Probability Sample
Study Population
Intensive Care Unit patients requiring both an arterial line and central venous line as part of their clinical care
Description
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
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
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Richard M Treger, M.D., VA Greater Los Angeles Healthcare System
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 Major Dates
Study Start
January 1, 2008
Primary Completion (Actual)
July 1, 2008
Study Completion (Actual)
July 1, 2008
Study Registration Dates
First Submitted
August 1, 2011
First Submitted That Met QC Criteria
August 1, 2011
First Posted (Estimate)
August 3, 2011
Study Record Updates
Last Update Posted (Estimate)
August 3, 2011
Last Update Submitted That Met QC Criteria
August 1, 2011
Last Verified
August 1, 2011
More Information
Terms related to this study
Other Study ID Numbers
- 193070
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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