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CompletedNCT03479671

Low Dose Fat-Induced Insulin Resistance

A Dose Finding Study for Fat-Induced Insulin Resistance in Healthy Volunteers

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
9 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
18 Years – 44 Years
Healthy volunteers
Accepted

Summary

The primary goal of this study is to determine the dose of fatty acids that acutely induces mild insulin resistance in healthy volunteers. We hypothesize that a low-dose of fatty acid infusion (Intralipid/heparin) will cause a mild insulin resistance. The dose of fatty acid infusion that reliably causes mild insulin resistance will be selected for use in future studies.

Detailed description

This study is designed to test the hypothesis that a low-dose of fatty acid infusion (Intralipid/heparin) will cause mild insulin resistance. This dose-finding study is critical for future studies on free-fatty acid induced insulin resistance. Healthy male and healthy female volunteers will undergo a 6 hour hyperinsulinemic-euglycemic clamp, in order to establish insulin sensitivity parameters in the presence of fatty acid co-infusion. The subjects will then return 1-3 weeks later, and undergo another 6 hour HIE clamp, this time in the presence of low-dose fatty acid co-infusion (30ml/hr). If this dose does not achieve \~25% reduction in the rate of glucose disposal, then the dose-confirmation study will be repeated 1-3 weeks later with a medium-dose fatty acid co-infusion (60ml/hr). A dose-response effect of fatty acids on insulin resistance has been demonstrated before, but not in the precise conditions of our study. This dose-finding study is critical because future studies require a reliable dose of fatty acid infusion, and the exact dose of fatty acid infusion that causes mild insulin resistance may be different in the conditions of our study.

Conditions

Interventions

TypeNameDescription
DRUGIntralipid, 20% Intravenous EmulsionFatty Acid Infusion, either in low-dose (30 ml/hr) or medium-dose (60 ml/hr)

Timeline

Start date
2020-01-01
Primary completion
2024-11-19
Completion
2024-11-19
First posted
2018-03-27
Last updated
2026-04-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03479671. Inclusion in this directory is not an endorsement.