What this study is
Diabetic kidney disease and cardiovascular disease remain the leading causes of morbidity and mortality in people with type 1 diabetes and are exacerbated with longer duration of diabetes and time outside goal glycemic range. Yet, type 1 diabetes is a complex disease with pathophysiology that extends beyond beta-cell injury and insulin deficiency to include insulin resistance and renal vascular resistance, factors that accelerate cardiovascular disease risk. We have shown that metformin improved peripheral insulin sensitivity and vascular stiffness in youth with type 1 diabetes on multiple daily insulin injections or standard insulin pumps. However, metformin's effect on kidney and endothelial outcomes, and the effects of type 1 diabetes technologies, with or without metformin, on any cardiovascular or kidney outcome, remains unknown. Automated insulin delivery systems combine an insulin pump, continuous glucose monitor, and control algorithm to modulate background insulin delivery and decrease peripheral insulin exposure while improving time in target range and reducing hypoglycemia. We hypothesize that automated insulin delivery systems, particularly when combined with metformin, may modulate renal vascular resistance and insulin sensitivity, thereby impacting cardiometabolic function. MANATEE-T1D is a randomized, double-blind, placebo-controlled trial of 4 months of metformin 2,000 mg daily in 40 youth aged 12-25 years with type 1 diabetes on automated insulin delivery systems vs. 20 control youth with type 1 diabetes on multiple daily injections plus a continuous glucose monitor or an insulin pump in manual mode plus a continuous glucose monitor which will assess for changes in calculated renal vascular resistance and gold standard measures of whole-body and adipose insulin sensitivity, arterial stiffness, and endothelial function.
What's being tested
- Metformin Hcl 1000Mg Tab
Intervention · DRUG
Agent used to modify insulin sensitivity
- Aminohippurate Sodium 20 % Injection
Intervention · DRUG
Diagnostic aid/agent used to measure renal plasma flow and calculate renal vascular resistance
- Iohexol 300 Mg/mL Injectable Solution
Intervention · DRUG
Diagnostic aid/agent used to measure glomerular filtration rate
- Placebo
Intervention · DRUG
Identical to Metformin Hcl 1000Mg Tab but without metabolic effects
Study details
- Sponsor
- Kalie Tommerdahl
- Conditions
- Type 1 Diabetes · Diabetic Kidney Disease · Cardiovascular Diseases · Endothelial Dysfunction · Insulin Sensitivity
- Enrolling
- 60 people
- Starts
- 2022-07-01
- Est. completion
- 2027-07-31
- Design
- Double-blind, randomized, parallel groups, Phase 1
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 12 Years – 25 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- T1D and using an automated insulin delivery system or multiple daily insulin injections/manual insulin pump plus continuous glucose monitor for > 6 months
- Age 12-25 years
- Use of an automated insulin delivery system or multiple daily insulin injections plus a continuous glucose monitor or an insulin pump in manual mode plus a continuous glucose monitor for > 6 months
- Hemoglobin A1c < 11%
- No recent episodes of diabetic ketoacidosis (DKA) or hyperglycemic hyperosmolar syndrome (HHS) (within 30 days)
- Pubertal (Tanner stage ≥ 2)
- Weight > 54 kg and BMI > 5th percentile for age and sex
You can't join if
- Blood pressure > 140/90 mm Hg
- Hemoglobin < 9 g/dL
- Estimated glomerular filtration rate < 60 mL/min/1.73 m2 or serum creatinine > 1.2 mg/dL or history of urinary albumin to creatinine ratio ≥ 300mg/g or history of acute kidney injury
- Use of anti-diabetic agents except insulin, angiotensin converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARB's), diuretics, daily non-steroidal anti-inflammatory drugs (NSAIDs) or aspirin, sulfonamides, procaine, thiazosulfone or probenecid
- Seafood or iodine allergy
- Pregnancy or breast feeding for females
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (2)
1 openSeattle Children's Hospital
Seattle, Washington, United States
- Kalie Tommerdahl, MD · Contact(206) 616-9015ktomme@uw.edu
- Kalie Tommerdahl, MD · Principal investigator
RecruitingChildren's Hospital Colorado/University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States
Active, not recruiting
Study team
Sponsor
Kalie Tommerdahl
Study ID 21-3483
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.