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Recruiting NCT06424015

NCT06424015 Insulin and Insulin Pulses During Fasting

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Clinical Trial Summary
NCT ID NCT06424015
Status Recruiting
Phase
Sponsor Mayo Clinic
Condition PreDiabetes
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2024-09-15
Primary Completion 2026-09-01

Eligibility & Interventions

Sex All sexes
Min Age 25 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Intralipid and heparinSaline

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2024-09-15 with a primary completion date of 2026-09-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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: * 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%

Contact & Investigator

Central Contact

Kim Osmundson, CCRP

✉ Osmundson.Kimberly@mayo.edu

📞 507-255-0907

Principal Investigator

Adrian Vella, MD

PRINCIPAL INVESTIGATOR

Mayo Clinic

Frequently Asked Questions

Who can join the NCT06424015 clinical trial?

This trial is open to participants of all sexes, aged 25 Years or older, up to 65 Years, studying PreDiabetes. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06424015 currently recruiting?

Yes, NCT06424015 is actively recruiting participants. Contact the research team at Osmundson.Kimberly@mayo.edu for enrollment information.

Where is the NCT06424015 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT06424015 clinical trial?

NCT06424015 is sponsored by Mayo Clinic. The principal investigator is Adrian Vella, MD at Mayo Clinic. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology