Vanderbilt University Medical Center
Nashville, Tennessee, 37209, United States
NCT Number: NCT06162715
The goal of this pilot clinical trial is to determine the effectiveness of Tirzepatide in patients with persistent obesity (BMI > 30) 12 months after bariatric surgery (Roux-en-Y Gastric Bypass). The investigators also aim to determine the frequency of side effects with Tirzepatide in this patient population. Patients who take tirzepatide 12 months after bariatric surgery will be compared to patients who continue with the current standard of care for patients who have previously undergone Gastric Bypass Surgery.
Interested in participating?
Request Info25 year–65 year
All sexes
Interventional
Phase 2 / Phase 3
Nashville, Tennessee, 37209, United States
Obesity affects nearly half of the U.S. population, impacting health outcomes including diabetes, cardiovascular risk, longevity, and quality of life. While bariatric surgery such as gastric bypass stands as the most effective intervention, 65% of individuals experience persistent obesity when undergoing surgical weight loss alone. Given the wide-ranging impact of obesity on health outcomes, a critical need exists to explore the efficacy of adjuvant weight loss therapies after gastric bypass surgery. Tirzepatide (TRZ), a type of glucagon-like peptide-1 receptor agonist, shows remarkable effectiveness in medical obesity with 25% weight loss after sustained therapy. However, nearly two-thirds of patients taking medications like TRZ have mild to moderate gastrointestinal (GI) symptoms, including nausea, vomiting, and abdominal pain. These medication side-effects could be a consequence of gastroparesis via vagal stimulation of the stomach, and may represent a major driver of weight loss. Limited data exist regarding use of these newer agents, such as TRZ, in patients who have undergone gastric bypass, which disrupts vagal nerves responsible for managing food transit and gastric emptying. This is a major and timely scientific gap in understanding whether gastric bypass surgery might mitigate these GI symptoms while allowing for enhanced weight loss with adjuvant TRZ use in the post-operative period. The investigators propose a pilot, phase II, open-label trial enrolling patients twelve months after gastric bypass with a nadir Body Mass Index ≥ 30 kg/m2. Study subjects will be randomized to either 24 weeks of TRZ or post-surgery standard of care. Subjects randomized to the standard of care arm will crossover to receive the intervention drug after 24 weeks of observation. Our proposal consists of two aims. First, the investigators will determine the impact of adjuvant TRZ administration on weight, total fat mass, and lean body mass in patients with a history of gastric bypass (Aim 1). Second, the investigators aim to investigate the frequency and severity of GI discomfort associated with TRZ utilizing a validated patient reported outcome questionnaire, and they will investigate the impact of TRZ on GI motility in patients with prior Gastric Bypass (Aim 2).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tirzepatide will be initiated 12 or 18 months (12 months + 24 weeks) after patients undergo Roux-en-Y Gastric Bypass. Patients will be started on the lowest dose of 2.5 mg and the dose increased every 6 weeks following an adaptive maximum dose titration protocol. Patients will then complete a final 4 weeks of the study drug.
Other names: Zepbound, Mounjaro
Patients randomized to the control arm will receive the standard of care for weight maintenance after gastric bypass including dietary guidance provided by the Vanderbilt Surgical Weight Loss handbook. This includes recommendations for 64 oz of fluids per day, ≥60 grams of protein/day, and daily bariatric multivitamins. Patients will continue to have access to dedicated bariatric dietitians, advanced practice providers, and surgeons on an ad hoc basis per patients' request.
Time frame: baseline to 24 weeks
Change in weight over time.
Time frame: baseline to 24 weeks
We will measure the average PAGI SYM score from 0 - 24 weeks in both arms.
Time frame: baseline to 24 weeks
Changes in fat mass
Time frame: baseline to 24 weeks
Changes in acetaminophen area under the curve in the intervention arm
Time frame: baseline to 24 weeks
Utilizing DXA, we will determine changes in lean body mass in both arms
Time frame: weeks 24 to 48
Degree of weight regain in intervention arm after discontinuation of TRZ
Time frame: baseline to 24 weeks
incidence of obesity remission (BMI < 30)
Time frame: baseline to 24 weeks.
Incidence of remission of Type 2 Diabetes, Hyperlipidemia, Hypertension
Time frame: baseline to 24 weeks
Changes in clinical obtained anthropometric measurements including waist circumference and waist-to-hip ratio
Time frame: baseline to 24 weeks.
Changes in DXA-proven body composition including lean body mass and ratio of lean body mass to fat mass
Time frame: baseline to 24 weeks
Time frame: baseline to week 24 and week 24 to week 28 (after TRZ discontinuation)
Determining evolution of PAGI-SYM scores across treatment in both arms and after discontinuation of TRZ in the intervetion arm.
Time frame: baseline to 24 weeks
difference in acetaminophen AUC between Intervention and control groups
Time frame: baseline to 24 weeks
change in intervention arm mixed meal AUC for Glucose, Insulin, and GLP-1
Time frame: baseline to 24 weeks
Incidence of missed doses, patient-driven drug discontinuation, patient withdrawal in intervention arm
Time frame: baseline to 48 weeks
Incidence of adverse events including emergency department visits, hospitalizations, and reoperations
Vanderbilt University Medical Center
Other
Acronym: GRABS-0
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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