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Effect of GLP-1 on Microvascular Insulin Responses in Type 1 Diabetes

Megadott ok: the study drug could not be obtained

Key facts

Where
Charlottesville, Egyesült ÁllamokSee the site
Phase
Korai 1. fázis

Where in Egyesült Államok

  • University of VirginiaCharlottesville, Egyesült ÁllamokNo longer taking part

Trial details

Who runs it
University of Virginia
Trial code
NCT04133922
Record updated
2022. március 22.
Original description
GLP-1 increases skeletal and cardiac microvascular perfusion and improves insulin's microvascular responses in human subjects with T1DM, leading to improved metabolic insulin responses, endothelial function, and increased muscle oxygenationRead full original descriptionShow less

GLP-1 increases skeletal and cardiac microvascular perfusion and improves insulin's microvascular responses in human subjects with T1DM, leading to improved metabolic insulin responses, endothelial function, and increased muscle oxygenation

Inclusion: History of type 1 diabetes, duration > 1 year; Age 18-40 years; HbA1c < 8.5%; BMI >/=18, <30 kg/m2; Using insulin for diabetes treatment only; On stable regimen of non-diabetic medications for the last 6 months, excluding oral contraceptives (OCP); All screening labs within normal limits or not clinical significant.

Exclusion: Pregnancy or currently breastfeeding 2) Smoking history within 6 months 3) History of microvascular (microalbuminuria, retinopathy, neuropathy) or macrovascular diabetes complications (coronary artery disease, stroke, peripheral vascular disease) 4) Taking vasoactive medications (i.e. calcium channel blockers, angiotensin-converting enzyme or renin inhibitors, angiotensin-receptor blockers, nitrates, alpha-blockers) 5) OCP use within 3 months or 1 month if menses has subsequently occurred 6) Known hypersensitivity to perflutren (contained in Definity© contrast) 7) Screening O2 saturation<90% 8) Anemia (hemoglobin <12 g/dL in women, hemoglobin <13 g/dL in men) 9) Diabetic ketoacidosis (DKA) on presentation to screening visits or study admission days; -.

ClinicalTrials.gov NCT04133922