- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01228968
Toward an Automated Method of Abdominal Fat Segmentation of MR Images
June 13, 2018 updated by: Washington University School of Medicine
Subjects will undergo a brief magnetic resonance (MRI) scan.
The resulting images will be used to compare two abdominal fat segmentation techniques.
The first technique is already validated and in use.
The second technique was recently developed and has not been validated.
The hypothesis is that the second technique will be the faster and more reliable of the two.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
9
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
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Saint Louis, Missouri, United States, 63110
- Washington University School of Medicine
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-
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 to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Subjects will have a wide range of body mass index and other physical characteristics.
Description
Inclusion Criteria:
- ambulatory
- cognitively sound
Exclusion Criteria:
- body mass index less than 18 or greater than 45 kilograms per square meter
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
Cohorts and Interventions
Group / Cohort |
|---|
|
Volunteers
Volunteers will have a range of body mass index from 19 - 45 kilogram per square meter.
In order to fit in the magnetic resonance scanner subjects must weigh less than 300 pounds.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visceral Fat Volume With Automated Analysis
Time Frame: five minutes
|
This is the measurement of Abdominal Visceral Fat in cubic centimeters as determined with a new automated segmentation program.
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five minutes
|
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Visceral Fat Volume With Manual Segmentation
Time Frame: five minutes
|
This is the measure of visceral fat found with our older manual segmentation method
|
five minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subcutaneous Fat Volume With Automated Analysis
Time Frame: five minutes
|
This is the volume of Abdominal Subcutaneous Fat in cubic centimeters as determined with new automated anatomical segmentation software.
|
five minutes
|
|
Subcutaneous Fat Volume With Manual Segmentation
Time Frame: five minutes
|
This is the volume of Abdominal Subcutaneous Fat in cubic centimeters as determined with the older manual segmentation technique.
|
five minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Samuel Klein, M.D., Washington University School of Medicine
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
October 1, 2010
Primary Completion (Actual)
February 1, 2011
Study Completion (Actual)
February 1, 2011
Study Registration Dates
First Submitted
October 25, 2010
First Submitted That Met QC Criteria
October 26, 2010
First Posted (Estimate)
October 27, 2010
Study Record Updates
Last Update Posted (Actual)
July 11, 2018
Last Update Submitted That Met QC Criteria
June 13, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MRImethods060229
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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