Insulin and Insulin Pulses During Fasting
Effect of Insulin and Insulin Pulses on Fasting Glucagon Secretion and on Glucose Metabolism in Subjects Without Type 2 Diabetes
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 25 Years to 65 Years
- Sex
- All sexes
- Healthy volunteers
- Accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study looks at how insulin and glucagon, two hormones, work to control blood sugar during fasting (not eating). It is for people whose blood sugar is normal or who have trouble keeping it in the normal range.
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Blood sugar after fasting is normal or above normal, and the body's ability to handle sugar is normal or reduced.
Who can't join
- HbA1c above 6.5%. This test measures average blood sugar over the past few months.
- Body mass index (BMI) of 35 or higher. BMI is a measure based on height and weight.
- Use of any medicine that lowers blood sugar, including metformin or sulfonylureas.
- A positive pregnancy test when joining the study or during the study.
- Past surgery in the upper belly, such as a stomach band or surgery on the stomach opening or its nerves.
- An active illness that affects the whole body, or cancer.
- Disease of large or small blood vessels that causes symptoms.
- Hematocrit below 35%. This means less than 35% of the blood is made up of red blood cells.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * people with normal or impaired fasting glucose and normal or impaired glucose tolerance Exclusion Criteria: 1. HbA1c \> 6.5% 2. BMI ≥ 35 Kg/M2 3. Use of any glucose-lowering agents including metformin or sulfonylureas. 4. For female subjects: positive pregnancy test at the time of enrollment or study 5. History of prior upper abdominal surgery such as adjustable gastric banding, pyloroplasty and vagotomy. 6. Active systemic illness or malignancy. 7. Symptomatic macrovascular or microvascular disease. 8. Hematocrit \< 35%
Study sites (1)
MN
- Mayo Clinic in Rochester · Rochester, MN 55905More trials in Rochester