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Semaglutide

Ozempic, Rybelsus, Wegovy

Quick Stats
Studies 78
Trials 100
Active Not Recruiting OBSERVATIONAL NCT05756764

Anti-obesity Pharmacotherapy and Inflammation

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

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

Detailed Description

This study aims to determine if weight loss by pharmacotherapy with liraglutide, semaglutide, or phentermine-topiramate promotes the reduction of pro-tumoral inflammatory cells Myeloid-derived suppressor cells (MDSC), simultaneously to the improvement of lipid profile (LDL-Cholesterol, HDL-Cholesterol, triglycerides, and free fatty acids) and concentration in the blood. Liraglutide, semaglutide, and phentermine-topiramate are FDA-approved medications to treat obesity and obesity-associated comorbidities. Twenty-four patients undergoing standard of care for anti-obesity treatment at VA Medical Center, and Tulane Center for Clinical Research (TCCR) will be recruited before initiation of pharmacotherapy as part of their standard of care and followed up to 6 months to compare the primary study variables.

Interventions

Name: Semaglutide
Type: DRUG
Description: Medication for weight loss
Name: Phentermine-Topiramate combination
Type: DRUG
Description: Medication for weight loss
Name: Phentermine
Type: DRUG
Description: Medication for weight loss
Name: Tirzepatide
Type: DRUG
Description: Medication for weight loss
Name: Topiramate
Type: DRUG
Description: Medication for weight loss
Name: Diethylpropion
Type: DRUG
Description: Medication for weight loss
Name: Naltrexone/Bupropion
Type: DRUG
Description: Medication for weight loss
Name: Liraglutide
Type: DRUG
Description: Medication for weight loss

Primary Outcomes

Measure: weight loss
TimeFrame: baseline and 24 weeks
Description: Weight Loss Percentage (Pounds lost divided by starting weight (in pounds) multiplied by 100)
Measure: MDSC in peripheral blood
TimeFrame: baseline and 24 weeks
Description: Changes in number of MDSC in blood
Measure: Levels of lipids in circulation
TimeFrame: baseline and 24 weeks
Description: Changes in concentration (mg/dL) of each type of lipids: LDL-Cholesterol, triglycerides, and free fatty acids

Trial Information

NCT ID

NCT05756764

Status

Active Not Recruiting

Study Type

OBSERVATIONAL

Sponsor

Louisiana State University Health Sciences Center in New Orleans

Last Updated

December 15, 2025

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