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Recruiting NCT06424106

NCT06424106 Effect of Glucagon on Fasting Insulin Secretion and Glucose Metabolism in Subjects Without Type 2 Diabetes

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Clinical Trial Summary
NCT ID NCT06424106
Status Recruiting
Phase
Sponsor Mayo Clinic
Condition PreDiabetes
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2025-04-01
Primary Completion 2027-07-01

Trial Parameters

Condition PreDiabetes
Sponsor Mayo Clinic
Study Type INTERVENTIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 25 Years
Max Age 65 Years
Start Date 2025-04-01
Completion 2027-07-01
Interventions
GlucagonGlucose

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Brief Summary

Fasting hyperglycemia contributes disproportionately to nonenzymatic glycosylation and the microvascular complications of type 2 diabetes. However, little is known about the regulation of glucose concentrations in the fasting state relative to what is known about the postprandial state. The proposed experiment is part of a series of experiments designed to establish how glucagon and insulin interact with their receptors to control fasting glucose in health and in prediabetes.

Eligibility Criteria

Inclusion Criteria: * Individuals with normal or impaired fasting glucose and normal or impaired glucose tolerance Exclusion Criteria: * HbA1c less than 6.5% * Use of any glucose-lowering agents including metformin or sulfonylureas. * For female subjects: positive pregnancy test at the time of enrollment or study * History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy. * Active systemic illness or malignancy. * Symptomatic macrovascular or microvascular disease.

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