Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
1 participants
INTERVENTIONAL
2020-12-14
2022-12-15
Brief Summary
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To address the hypothesis, the investigators would like to assess brown fat distribution and activity in this subject.
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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One subject with possible Luft's disease
18F-FDG will be administered I.V., approximately 1 hour prior to PET/CT scan.
18F FDG PET/CT
18F FDG PET/CT imaging (fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography).
Interventions
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18F FDG PET/CT
18F FDG PET/CT imaging (fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography).
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
9 Years
18 Years
ALL
No
Sponsors
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The Hospital for Sick Children
OTHER
Responsible Party
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Andreas Schulze
Principal Investigator
Principal Investigators
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Andreas Schulze, MD
Role: PRINCIPAL_INVESTIGATOR
The Hospital for Sick Children
Locations
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The Hospital for Sick Children
Toronto, , Canada
Countries
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Other Identifiers
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1000061502
Identifier Type: -
Identifier Source: org_study_id