Effects of Ondansetron on Gastrointestinal Sensorimotor Dysfunctions in Diabetes Mellitus and Dyspepsia

• Status: Recruiting
• Trial end date: 2026-03-01
• Target enrollment: 0
• Participant gender: All

Summary

Researchers are trying to understand why people with indigestion and diabetes mellitus have gastrointestinal symptoms and in particular to understand whether symptoms are related to increased sensitivity to nutrients in the small intestine. As part of this investigation, a medication called ondansetron will also be studied to determine its effects on gastrointestinal function and associated symptoms.

• Phase: Phase 2
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Mayo Clinic
• Collaborator: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
• Treatments: Ondansetron

Criteria

Inclusion Criteria:

• Healthy male or non-pregnant, non-breastfeeding female volunteers;

• 18-75 years old;

• Able to provide written informed consent before participating in the study

• Able to communicate adequately with the investigator and to comply with the requirements for the entire study; including the willingness and ability to consume the components of the test meals

• Symptoms of dyspepsia (i.e., early satiety, postprandial discomfort, nausea, vomiting, regurgitation)

• Patients in the DM group will also require Type 1 or 2 DM of ≥ 3 years duration; in patients with type 2 DM, the dyspepsia symptoms should have begun or worsened after DM was diagnosed

Exclusion Criteria:

• Major abdominal surgery (i.e., appendectomy, cholecystectomy, tubal ligation, hysterectomy, herniorrhaphy, and limited colonic resection are permissible)

• Clinical evidence (including physical exam and EKG) of significant cardiovascular, respiratory, renal, hepatic, gastrointestinal, hematological, neurological, psychiatric or other disease that may interfere with the objectives of the study and/or pose safety concerns

• Current use of opiates, alpha adrenergic agonists, metoclopramide, monoamine oxidase inhibitors, more than one serotonergic medication, and high doses of anticholinergic agents (eg, amitriptyline greater than 50 mg daily). If medically safe, these drugs may be discontinued for four half lives prior to study assessments.

• Treatment with GLP-1 agonists and amlyin which cause vagal blockade and may affect central processing of pain

• Bleeding or clotting disorders or medications that increase risk of bleeding from mucosal biopsies

• Positive tissue transglutaminase antibodies (TTG),

• Pregnant or breast-feeding females

• Known intolerance or allergy to eggs

• Poor peripheral venous access, if central venous access is not available

• Any other condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study

• History of Long QT Syndrome or prolonged QT interval (i.e., corrected QT interval > 480 ms)

• Current symptoms of a functional gastrointestinal disorder assessed by questionnaire

• Severe vomiting that would preclude tube placement or participation in the study

• Structural cause for symptoms by endoscopy within the past 12 months

• Patients with gastric pacemakers