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NCT01922960 Clinical Trial

Microcirculatory Assessment in Patients With Trauma and Severe Burns

Trauma Clinical Trial

Official title:
Microcirculatory Assessment in Patients With Trauma and Severe Burns

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01922960
Other study ID # 12-092
Secondary ID
Status Withdrawn
Phase N/A
First received June 27, 2013
Last updated November 27, 2017
Start date April 7, 2012
Est. completion date February 2014

Study information
Verified date November 2017
Source University of South Alabama
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Predict the development of multiple organ failure in patients with trauma and severe burns.

Description:

Microvascular alterations are frequently seen in patients with sepsis, trauma, burns and those who are hemodynamically uncompensated(Shock).

The use of the Microscan is a non-invasive approach to visualize and assess impaired mucosal microcirculation in order to identify early on patients who are predisposed for MOF (multiple organ failure)

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date February 2014
Est. primary completion date February 2014
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients with severe burns/trauma ages 19-80. Patients undergoing elective abdominal or cardiothoracic surgery ages 19-69 years old

Exclusion Criteria:

- Patients undergoing elective surgery < 19 years old.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• micro-imaging
micro-imaging

Locations
Country Name City State
United States University of South Alabama Medical Center Mobile Alabama

Sponsors (1)
Lead Sponsor Collaborator
University of South Alabama

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary dysfunctional capillary density correlates with development of multiple organ failure approximately 1 year to assess outcome measure
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