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University of Missouri

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Columbia, Missouri 65201

Global Leader in Obesity

Global Leader in Diabetes

Conducts research for Motor Skills

Conducts research for Insomnia

Conducts research for I Am A Healthy Volunteer

301 reported clinical trials

30 medical researchers

Photo of University of Missouri in ColumbiaPhoto of University of Missouri in ColumbiaPhoto of University of Missouri in Columbia

Summary

University of Missouri is a medical facility located in Columbia, Missouri. This center is recognized for care of Obesity, Diabetes, Motor Skills, Insomnia, I Am A Healthy Volunteer and other specialties. University of Missouri is involved with conducting 301 clinical trials across 591 conditions. There are 30 research doctors associated with this hospital, such as Puja Nistala, Christos Papageorgiou, Katie Murray, DO, MS, SACS, and Dima Dandachi, MD.

Top PIs

Clinical Trials running at University of Missouri

Obesity

Diabetes

Cancer

Stroke

Age-Related Macular Degeneration

Insomnia

Asthma

Breast Cancer

Autism

Dementia

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GLP-1 Agonists

for Obesity

Glucagon-like peptide 1 (GLP-1) is a hormone that helps regulate blood glucose levels through improved insulin sensitivity and release of insulin from the pancreas, control hunger, induce satiety and plays a role in the metabolic health of a person. GLP-1 receptor agonists (GLP1-RAs) have been shown to be effective in achieving weight loss in patients with type 2 diabetes while improving blood glucose control. Bariatric surgical procedures have been shown to be effective in treating obesity as well as superior to best medical therapy for treatment of diabetes not just through restriction of calories but also through a positive impact in modifications of gut hormones, changes in circulating bile acids, modifications in the gut microflora as well as other undefined mechanisms. The combined benefits of GLP1-RAs with bariatric surgery have only been studied to a limited effect. In this randomized trial, the effects of continuation or discontinuation of GLP1-RA therapy in patients undergoing bariatric surgery will be determined. We will compare changes in weight, metabolic determinants including circulating bile acids and gut microbiome, psychological determinants of eating behavior, and adverse side effects in patients who continue vs discontinue therapy. Given differences in metabolic and clinical outcomes in patients undergoing vertical sleeve gastrectomy (VSG) and Roux-en-Y gastric bypass (RYGB), both surgical groups will be examined. The study will be conducted at a high volume bariatric surgical program where patients will undergo randomization at the time of final clinic visit prior to surgery to continue or discontinue GLP1-RA. It is hypothesized that participants who continue GLP1-RA therapy after bariatric surgery will lose more weight with improved blood glucose control than those who discontinue therapy. Furthermore, changes in gut microbiome and circulating bile acids, known determinants of metabolic health, will be modified to a differential extent in those who are on GLP1-RAs vs those where GLP1-RAs are discontinued. Understanding the role these medications play in not only clinical outcomes after metabolic surgery but potential metabolic mechanisms by which surgery improves patient's metabolic health could help people with obesity and type 2 diabetes make informed decisions about their treatment options as well as advise providers on the continuation of these medications in the perioperative and postoperative period.

Recruiting

3 awards

Phase 4

10 criteria

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Vascular Response Study in Obesity

for

The purpose of this project is to examine key mechanisms contributing to sex-differences in hypoxic vasodilation and the impact of obesity, with particular emphasis on the sympathetic nervous system.

Recruiting

3 awards

Phase < 1

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Comprehensive Multidisciplinary Care

for Obesity

This project will compare two training approaches for US Preventive Services Task Force recommended obesity care in Federally Qualified Health Centers (FQHC) across four aims. Aim 1 compares patient-level effectiveness \[i.e., patient relative weight change and the proportion of patients who achieve clinically significant weight loss\]. Aim 2 compares reach (patient treatment utilization). Aim 3 compares primary care provider (PCP) referrals to USPSTF-recommended care at 12 (adoption) and 24 months (maintenance) and short- and long-term changes in provider obesity care competencies . Aim 4 compares implementation and service costs.

Recruiting

1 award

N/A

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