Amino acids may change how the body controls blood sugar
NCT ID NCT05264727
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how amino acids (building blocks of protein) affect the release of glucagon and insulin compared to sugar alone. Researchers will test 30 adults who are healthy, have type 2 diabetes, or are obese. The goal is to better understand these hormone responses, not to provide a treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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30 people
The number who actually took part.
- Started
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May 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria - Obese Subjects with Type 2 Diabetes: * HbA1c ≤ 8.5% (type 2 diabetic subjects). * HbA1c ≤ 6.5% (obese and lean subjects). * BMI ≥ 28 Kg/M\^2 (Obese subjects with and without type 2 diabetes). * BMI ≤ 25 Kg/M\^2 (Lean subjects without type 2 diabetes). * Use of sulfonylureas or metformin only (type 2 diabetec subjects). * For female subjects: negative pregnancy test at the time of enrollment or study. * No history of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy. * No active systemic illness or malignancy. * No symptomatic macrovascular or microvascular disease. * No 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 negative AUDIT questionnaire. Exclusion Criteria - Obese Subjects with Type 2 Diabetes: * HbA1c ³ 8.5% * BMI ≤ 28 Kg/M2 * Use of insulin or agents other than sulfonylureas or metformin. * 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. * 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. Inclusion Criteria - Obese Subjects without Type 2 Diabetes: * BMI ≥ 28 Kg/M2. * \> 5% liver fat content, as determined by MRI using the proton density fat fraction (PDFF) technique. Exclusion Criteria - Obese Subjects without Type 2 Diabetes: * HbA1c ≥ 6.5% * BMI ≤ 28 Kg/M2 * 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. * 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. Inclusion Criteria - Lean subjects without Diabetes: \- BMI ≤ 25 Kg/M\^2). Exclusion Criteria - Lean Subjects without Diabetes: * HbA1c ≥ 6.5%. * BMI ≥ 25 Kg/M\^2. * 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. * 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. * Liver fat content ≥ 5% as determined by MRI using the proton density fat fraction (PDFF) technique.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Mayo Clinic Rochester
Rochester, Minnesota, 55905, United States
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Other studies related to the condition(s) this trial covers.
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