Myeloid to Adipocyte Transdifferentiation in Human Cells
NCT ID: NCT02654925
Last Updated: 2021-06-24
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
59 participants
OBSERVATIONAL
2016-03-31
2021-06-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
OTHER
Study Groups
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Young Men
men 21-40 years of age
Adipose Tissue Biopsy
Young Women
women 21-40 years of age; young women will be premenopausal and eumenorrheic, not on hormonal contraceptive therapy.
Adipose Tissue Biopsy
Older Men
men 55-100 years of age
Adipose Tissue Biopsy
Older Women
women 55-100 years of age; older women will be postmenopausal who are at least 12 months past the final menstrual period (FMP).
Adipose Tissue Biopsy
Interventions
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Adipose Tissue Biopsy
Eligibility Criteria
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Inclusion Criteria
* Older women will be postmenopausal who are at least 12 months past the final menstrual period (FMP);
* Young women will be premenopausal and eumenorrheic, not on hormonal contraceptive therapy;
* Body Mass Index (BMI) 22-35 kg/m2;
* Non-active to moderately active (vigorous exercise ≤ 3 days/wk lasting \< 30 min).
Exclusion Criteria
* On blood thinners, aspirin, or NSAIDs that cannot be withheld for the biopsy;
* Prior history of allergies to local anesthetics;
* Current use of hormones, or glucose lowering medication;
* Currently engaged in a vigorous exercise or diet program;
* Currently gaining or losing weight or using weight loss drugs;
* Type 2 diabetes (past/current diagnosis or treatment);
* Diagnosis of uncontrolled metabolic disorders (e.g., thyroid);
* History of severe obesity BMI ≥ 40 or significant weight loss (≥ 50 lbs);
* Postmenopausal - hormonal menopausal therapy use currently or in the previous 6 months;
* Premenopausal - irregular menstrual cycles defined as 2 or more missed cycles in the previous year, pregnant or planning to become pregnant during the study timeline (urine pregnancy test will be performed before DEXA \[dual energy x-ray absorptiometry\] scan is completed).
21 Years
100 Years
ALL
Yes
Sponsors
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University of Colorado, Denver
OTHER
Responsible Party
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Principal Investigators
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Kathleen M Gavin, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Colorado Denver Anschutz Medical Campus
Locations
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University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States
Countries
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Other Identifiers
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15-1779
Identifier Type: -
Identifier Source: org_study_id
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