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Enrolling by Invitation

NCT Number: NCT06162715

GLP-1 Receptor Agonists Post-Bariatric Surgery (GRABS) Pilot Trial

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.

Enrolling by Invitation

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Key information

Age range

25 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Vanderbilt University Medical Center

Nashville, Tennessee, 37209, United States

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject must be able to understand and provide informed consent.
  • BMI > 30 12 months after bariatric surgery.
  • Age > 25 and < 65
  • Patients undergoing primary Roux-en-Y Gastric Bypass

Exclusion criteria

  • Inability or unwillingness of a subject to give written informed consent or comply with the study protocol.
  • Diagnosis of type I Diabetes
  • Revisional bariatric surgery (prior adjustable gastric band, sleeve gastric, vertical banded gastroplasty).
  • Use of medications for type 2 di
  • Hemoglobin A1c > 8.5 in last 3 months.
  • Patient-reported Tobacco, e-cigarette, or smoked marijuana use within 12 months As this would preclude patients from undergoing bariatric surgery.
  • Personal history of pancreatitis as determined by history.
  • Personal or family history of medullary thyroid cancer by history or multiple endocrine neoplasia syndrome type 2
  • Pregnancy by urine testing, current lactation, or plans to become pregnant during the study period.
  • Use of systemic glucocorticoids in the past 28 days
  • Myocardial infarction, unstable angina, stroke, or heart failure (NYHA class II) within 1 year by history.
  • History of solid organ transplant.
  • History of physician-diagnosed malignancy (other than excised non-melanoma skin cancer) in the past 5 years.
  • Current uncontrolled hypertension (systolic >150, diastolic >90) or untreated hyperthyroidism.
  • Current, diagnosed, or self-reported drug or alcohol abuse that, in the opinion of the investigator, would interfere with the subject's ability to comply with study requirements.
  • Screening creatinine elevation with EGFR < 60 at time of randomization.
  • Tobacco use in last 12 months
  • Pregnancy
  • Prisoners
  • Unable or unwilling to follow-up
  • Unable to understand English/Spanish

Treatment and study plan

Tirzepatide

Drug

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

Standard of Care post-gastric bypass

Other

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.

Primary outcomes

  1. Weight loss

    Time frame: baseline to 24 weeks

    Change in weight over time.

  2. Gastrointestinal symptoms

    Time frame: baseline to 24 weeks

    We will measure the average PAGI SYM score from 0 - 24 weeks in both arms.

Secondary outcomes

  1. Change in body composition

    Time frame: baseline to 24 weeks

    Changes in fat mass

  2. Acetaminophen Area Under the Curve

    Time frame: baseline to 24 weeks

    Changes in acetaminophen area under the curve in the intervention arm

  3. Lean body mass

    Time frame: baseline to 24 weeks

    Utilizing DXA, we will determine changes in lean body mass in both arms

Other outcomes

  1. weight regain after TRZ discontinuation

    Time frame: weeks 24 to 48

    Degree of weight regain in intervention arm after discontinuation of TRZ

  2. Obesity remission

    Time frame: baseline to 24 weeks

    incidence of obesity remission (BMI < 30)

  3. Remission of pre-existing comorbidities

    Time frame: baseline to 24 weeks.

    Incidence of remission of Type 2 Diabetes, Hyperlipidemia, Hypertension

  4. change in anthropometric measurements

    Time frame: baseline to 24 weeks

    Changes in clinical obtained anthropometric measurements including waist circumference and waist-to-hip ratio

  5. changes in body composition

    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

  6. Change in PAGI-SYM sub-scale scores

    Time frame: baseline to 24 weeks

    • heartburn/regurgitation, 2. nausea/vomiting, 3. postprandial fullness, 4. bloating, 5. upper and lower abdominal pain
  7. change in PAGI-SYM scores in the TRZ arm

    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.

  8. Difference in acetaminophen AUC between groups

    Time frame: baseline to 24 weeks

    difference in acetaminophen AUC between Intervention and control groups

  9. Changes in response to mixed meal tolerance test

    Time frame: baseline to 24 weeks

    change in intervention arm mixed meal AUC for Glucose, Insulin, and GLP-1

  10. Medication adherence

    Time frame: baseline to 24 weeks

    Incidence of missed doses, patient-driven drug discontinuation, patient withdrawal in intervention arm

  11. Adverse events and healthcare resource utilization

    Time frame: baseline to 48 weeks

    Incidence of adverse events including emergency department visits, hospitalizations, and reoperations

Sponsors and collaborators

Lead sponsor

Vanderbilt University Medical Center

Other

Registry information

Acronym: GRABS-0

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Dec 8, 2023
Registry last updated
Jun 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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