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Taking people in United StatesPhase 2

Tests dulaglutide for blood vessel health in type 1 diabetes

Tests dulaglutide against placebo in adults with type 1 diabetes.

Plain-language title generated from the registry record
Registry title: Therapeutic Strategies for Microvascular Dysfunction in Type 1 Diabetes

Key facts

Where
Orlando, United StatesSee the site
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 40 years old?

Source: NCT05478707, who can take part

Where in United States

  • AdventHealth Translational Research InstituteOrlando, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
AdventHealth Translational Research Institute
Trial code
NCT05478707
Record updated
15 October 2026
Original description
The investigators will test the hypothesis that, in adults with type 1 diabetes (T1D), glucagon-like peptide-1 receptor agonism (GLP-1RA, i.e. dulaglutide) enhances insulin-mediated skeletal muscle microvascular perfusion via attenuating endothelial oxidative stress and thereby improving endothelial function.Read full original descriptionShow less

Therapeutic Strategies for Microvascular Dysfunction in Type 1 Diabetes

The investigators will test the hypothesis that, in adults with type 1 diabetes (T1D), glucagon-like peptide-1 receptor agonism (GLP-1RA, i.e. dulaglutide) enhances insulin-mediated skeletal muscle microvascular perfusion via attenuating endothelial oxidative stress and thereby improving endothelial function.

Inclusion: History of type 1 diabetes, duration > 5 years; Age 18-40 years; HbA1c < 8.5%; BMI 19-34.9 kg/m2; Using insulin for diabetes treatment only (multiple daily injections or insulin pump with or without sensor augmentation); On stable regimen of non-diabetic medications for the last 6 months; All screening labs within normal limits or not clinically significant - English or Spanish speaking.

Exclusion: History of microvascular (microalbuminuria, retinopathy, neuropathy) or macrovascular diabetes complications (coronary artery disease, stroke, peripheral vascular disease) as well as clinically significant cardiac arrhythmias or conduction disorders; Known hypersensitivity to perflutren (contained in Definity© contrast); Musculoskeletal condition preventing participation in exercise testing or exercise training; Acute or unstable disease other than T1D; History of gastroparesis, severe gastroesophageal reflux, pancreatitis, personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type 2; Taking vasoactive medications (i.e. calcium channel blockers, angiotensin-converting enzyme or renin inhibitors, angiotensin-receptor blockers, nitrates, alpha-blockers); Anemia (hemoglobin <12 g/dL in women, hemoglobin <13 g/dL in men), eosinophilia (absolute eosinophil count >500 cells/microliter) leukopenia (total white blood cells <4,000 cells/microliter); Pregnancy or currently breastfeeding; Smoking history within 6 months; Screening O2 saturation <90%; Hypoglycemia unawareness; Diabetic ketoacidosis (DKA) on presentation to screening visits or study admission days; Hospital admission for DKA within 1 year.

ClinicalTrials.gov NCT05478707