RECRUITING

Impact GLP-1 Agonists Following Bariatric

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Biometabolic Impact of Continuation of GLP-1 Agonists Following Bariatric

Quick Facts

Study Start:2024-02-01
Study Completion:2028-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06132477

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Greater than 18 years of age
  2. 2. Participation in care by one of the surgeons at MU Health Care
  3. 3. Undergoing surgical weight loss through the Weight Management and Metabolic Center
  4. 4. Body mass index of 30-80 kg/m2
  5. 5. Meet insurance criteria, as set forth by the patient's insurance policy, to qualify for coverage for weight loss surgery or as a self-pay patient for the weight loss procedure
  6. 6. Planned laparoscopic Roux-en-Y gastric bypass, sleeve gastrectomy, revisional weight loss surgery, or duodenal switch or modification of. If patients are not willing to be randomized they will not be enrolled as randomized but can still participate having samples collected.
  7. 7. Willingness to have blood collected before and after surgical procedure at defined points or at minimum have clinical data collected.
  8. 8. Willingness to have clinical data entered into a prospective database
  9. 9. Additional specimens collected as stated in the protocol will be offered but collection not mandated.
  10. 5. Taking a GLP-1 agonist as part of their routine medical care apart from any planned surgical procedure. The current standard of care regarding continuation or discontinuation of GLP-1 agonists has not been established and is at the discretion of members of the patient's medical team but to be included the patient and medical care team must be willing to continue or discontinue the GLP-1 agonist after surgery depending on the randomized group.
  1. 1. Pregnant patient
  2. 2. Desire to not participate
  3. 3. Age less than 18
  4. 4. Patient fails to fulfill insurance mandated criteria and is not interested in paying cash for their procedure
  5. 5. Not taking a GLP-1 agonist as part of standard medical care
  6. 6. Unwilling to follow-up at required postoperative visits
  7. 7. Unwilling to stop GLP-1 agonist if randomized into group to stop GLP-1 agonist or unwilling to continue the GLP-1 agonist if randomized into that respective group. If chooses to continue or discontinue the medication apart from randomization the patient can still participate as a non-randomized participant

Contacts and Locations

Study Contact

Lori Wilcox, EdD, MS
CONTACT
573-882-9500
muresearchirb@missouri.edu

Principal Investigator

Andrew Wheeler, MD
PRINCIPAL_INVESTIGATOR
University of Missouri-Columbia

Study Locations (Sites)

University of Missouri Hospital
Columbia, Missouri, 65201
United States

Collaborators and Investigators

Sponsor: University of Missouri-Columbia

  • Andrew Wheeler, MD, PRINCIPAL_INVESTIGATOR, University of Missouri-Columbia

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-01
Study Completion Date2028-07

Study Record Updates

Study Start Date2024-02-01
Study Completion Date2028-07

Terms related to this study

Keywords Provided by Researchers

  • glp-1 agonist
  • Morbid Obesity
  • Bariatric Surgery
  • Metabolic syndrome
  • Diabetes Mellitus
  • Hypertension
  • Obstructive Sleep Apnea

Additional Relevant MeSH Terms

  • Morbid Obesity
  • Metabolic Syndrome
  • Diabetes Mellitus
  • Hypertension
  • Obstructive Sleep Apnea of Adult