Obesity Clinical Trial
Official title:
The Effects of Metabolic & Bariatric Surgery on Lipid Metabolism, Myeloid-Derived Suppressor Cells, and Cancer Cell Biology
This study aims to determine the relationship between lipid kinetics changes and blood immunosuppressive cells by metabolic surgery in two patient cohorts.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | December 31, 2025 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 35 Years to 60 Years |
Eligibility | For an eligible subject, all the following must be answered "yes": - Biological female sex - Age >=35 and <=60 years (including pre- and postmenopausal) - Self-reported white or black race - The study will enroll approximately 50% white and 50% black subjects - Body mass index >/=40 kg/m2 - Have a diagnosis of hyperlipidemia (high triglycerides and LDL-cholesterol) or in treatment with any medication for hyperlipidemia at enrollment - Ability to provide written informed consent - Allow the collection and storage of biospecimens and data for future use - Not having yet started the pre-op liquid diet before the bariatric surgery For an eligible subject, all the following must be answered "no": - Have type one or type two diabetes - Use of anti-inflammatory medications, such as glucocorticoids or non-steroidal anti-inflammatory medications, within the past 15 days - Use of medication approved for obesity management, including, but not limited to, phentermine-topiramate (Qsymia), orlistat (Xenical), naltrexone-bupropion (Contrave), liraglutide (Saxenda), and semaglutide (Wegovy) - History of cancer of any type - History of chronic conditions known to cause inflammation, such as tuberculosis, autoimmune disease, and human immunodeficiency virus - An acute history (within the past 60 days) or confirmed or suspected SARS-CoV-2 (COVID-19) infection - Currently pregnant, breastfeeding, or planning to become pregnant within the next 52 weeks - Currently participating in another study with competing outcomes - Any other situation that, in the opinion of the investigator, would negatively impact subject safety or successful compliance with the protocol |
Country | Name | City | State |
---|---|---|---|
United States | Pennington Biomedical Resarch Center | Baton Rouge | Louisiana |
Lead Sponsor | Collaborator |
---|---|
Pennington Biomedical Research Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in insulin-inhibited adipose tissue lipolysis | Baseline, week 52 | ||
Primary | Change in the number of circulating myeloid-derived suppressor cells | Baseline, week 52 |
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