Trauma Clinical Trial
Official title:
Use of Diffuse Optical Spectroscopy for Evaluation of the Trauma/Critically Care Patients
NCT number | NCT00581295 |
Other study ID # | 20139435 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 2007 |
Est. completion date | April 2011 |
Verified date | October 2022 |
Source | University of California, Irvine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Trauma remains the leading cause of death and disability for Americans age 1-44. Trauma can cause internal bleeding, and this bleeding is often hard to detect without sophisticate tests that take time to complete and analyze. In addition, internal bleeding, including bleeding into the lung and chest cavity, as well as other blood loss, happens in many critically ill patients. For example, for hemorrhage, it is very difficult to detect active hemorrhage and to determine optimal rates of fluid and blood resuscitation. Diffuse optical spectroscopy has the potential to accurately assess adequacy of tissue perfusion, oxygenation, tissue oxygen extraction, and cytochrome oxidation states that may be critical to optimal treatment, end- organ preservation, and survival.
Status | Completed |
Enrollment | 93 |
Est. completion date | April 2011 |
Est. primary completion date | April 2011 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult age 18 years or older, male or female - Trauma/Critical Care patient Exclusion Criteria: - Subject is not Trauma/Critical Care patient |
Country | Name | City | State |
---|---|---|---|
United States | Beckman Laser Institute,University of California, Irvine | Irvine | California |
United States | Trauma/Critical Care Units, UCI Medical Center | Orange | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Irvine | Beckman Laser Institute University of California Irvine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The ability to noninvasively diagnose conditions in the intensive care unit, or in battlefield conditions. | 5 to 60 seconds |
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