Study Results
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View full resultsBasic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2019-03-20
2022-10-02
Brief Summary
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Subjects currently living in the Chicago metropolitan area and meet inclusion/exclusion criteria will be considered for enrollment.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Experimental Group
LOGIQ P6 Diagnostic Ultrasound
Ultrasound measurements of subcutaneous fat thickness
Interventions
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LOGIQ P6 Diagnostic Ultrasound
Ultrasound measurements of subcutaneous fat thickness
Eligibility Criteria
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Inclusion Criteria
* Subjects are in good health as judged by the investigator.
* Subjects with Body Mass Index (BMI) between 18-29.99.
* Subjects who are willing and have the ability to understand and provide informed consent for participation in the study and are able to communicate with the investigator
Exclusion Criteria
* Pregnant or breast feeding
* Uncooperative patients or patients with neurological disorders who are incapable of following directions
* Subjects who are unable to understand the protocol or give informed consent (including non-English speaking patients)
18 Years
85 Years
ALL
No
Sponsors
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Northwestern University
OTHER
Responsible Party
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Murad Alam
Principal Investigator
Principal Investigators
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Murad Alam, MD
Role: PRINCIPAL_INVESTIGATOR
Northwestern University
Locations
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Northwestern University Department of Dermatology
Chicago, Illinois, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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STU002089391
Identifier Type: -
Identifier Source: org_study_id
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