Anti-obesity Pharmacotherapy and Inflammation
Running, not enrolling
Conditions studied: Obesity
In brief
This study evaluates the relationship between weight loss, circulating inflammatory markers and lipids from 24 patients before and after 6 months of pharmacotherapy as a standard of care for anti-obesity treatment
Key facts
- Study ID
- NCT05756764
- Run by
- Louisiana State University Health Sciences Center in New Orleans
- People needed
- 30
- Starts
- 2023-06-01
- Expected to finish
- 2026-02-20
- Last updated by the study team
- 2025-09-09
Who can join
Age: 35 and older, up to 60. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Body mass index (BMI): over 30 kg/m2
- Age: 35 to 60 years old
You may not qualify if…
- Taking medications with anti-inflammatory properties like glucocorticoids, prednisone, or non-steroidal anti-inflammatory medications, such as aspirin or Motrin Subjects on medications for long-term weight management such as phentermine-topiramate (Qsymia), orlistat (Xenical), naltrexone-bupropion (Contrave), and the glucagon-like peptide-1 receptor agonists such as liraglutide (Saxenda), and semaglutide (Wegovy).
- Prior history of cancer
- Having any clinical symptoms of systemic inflammation, acute infections such as Coronavirus disease 2019, or chronic diseases such as cancer, tuberculosis, autoimmune disease, and AIDS
- An adult unable to consent
- Prisoner
- Pregnancy or breastfeeding women
Where it is running
- LSU Clinical & Translational Research Center (CTRC - - LSUHSC-NO — New Orleans, Louisiana, United States
- Ochsner Health System - Biospecimen — New Orleans, Louisiana, United States
Full record on ClinicalTrials.gov
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