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The Effects of Glucagon on Hepatic Metabolism in People With Type 2 Diabetes After Caloric Restriction

Launched by ADRIAN VELLA · Aug 11, 2022

Trial Information

Current as of August 27, 2025

Recruiting

Keywords

Glucagon Insulin Resistance Caloric Restriction Hepatic Steatosis Amino Acid Metabolism

ClinConnect Summary

This clinical trial is exploring how caloric restriction, which means eating fewer calories, affects the way glucagon works in the liver of people with type 2 diabetes. Glucagon is a hormone that helps control blood sugar levels. The researchers want to see if eating less can improve the liver's ability to manage amino acids, carbohydrates, and fats in people with type 2 diabetes. This study is particularly focused on comparing the effects of caloric restriction on glucagon's actions to what happens in people with type 2 diabetes who are not on a caloric restriction plan.

To participate in this study, you should be between 18 and 75 years old, have type 2 diabetes that is managed with diet or oral medications, and have a body mass index (BMI) of 28 or higher. However, individuals with certain health issues, prior upper abdominal surgeries, or specific medical conditions may not be eligible. If you join the trial, you can expect to be part of a controlled environment where your dietary intake and health will be monitored. This research aims to provide more insights into how dietary changes can help manage diabetes effectively.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • We will recruit up to 20 weight-stable, subjects with type 2 diabetes
  • BMI ≥ 28 Kg/M2
  • Diabetes is managed by diet alone or a combination of oral agents
  • Exclusion Criteria:
  • History of prior upper abdominal surgery e.g. gastric banding, pyloroplasty, vagotomy.
  • Active systemic illness or malignancy.
  • Symptomatic macrovascular or microvascular disease.
  • Contraindications to MRI (e.g. metal implants, claustrophobia).
  • Hematocrit \< 35%
  • TSH \< 0.4 or \> 5.5.
  • Consumption of \> 2 alcohol drinks per day or \> 14 per week or a positive AUDIT questionnaire.

About Adrian Vella

Adrian Vella is a distinguished clinical trial sponsor known for his commitment to advancing medical research and innovation. With a strong background in endocrinology and metabolic diseases, Dr. Vella leads initiatives that focus on understanding and developing therapeutic interventions for conditions such as diabetes and obesity. His expertise encompasses the design and execution of clinical studies, ensuring adherence to regulatory standards and ethical guidelines. Through collaborative efforts with academic institutions and industry partners, Adrian Vella aims to translate scientific discoveries into effective treatments that improve patient outcomes and enhance healthcare practices.

Locations

Rochester, Minnesota, United States

Patients applied

0 patients applied

Trial Officials

Adrian Vella

Principal Investigator

Mayo Clinic

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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