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NCT Number: NCT05065372

MANATEE-T1D: Metformin ANd AutomaTEd Insulin Delivery System Effects on Renal Vascular Resistance, Insulin Sensitivity, and Cardiometabolic Function in Youth With Type 1 Diabetes

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Metformin Hcl 1000Mg Tab

Drug

Agent used to modify insulin sensitivity

Other names: Fortamet, Glucophage, Glumetza, Riomet

Aminohippurate Sodium 20 % Injection

Drug

Diagnostic aid/agent used to measure renal plasma flow and calculate renal vascular resistance

Other names: Sodium 4-amino hippurate (PAH) injection 20% (2g/10 mL), Para-aminohippurate, Aminohippuric acid

Iohexol 300 Mg/mL Injectable Solution

Drug

Diagnostic aid/agent used to measure glomerular filtration rate

Other names: Omnipaque 300

Placebo

Drug

Identical to Metformin Hcl 1000Mg Tab but without metabolic effects

Primary outcomes

  1. Renal vascular resistance

    Time frame: 4 months

    Renal plasma flow will be measured by para-aminohippurate clearance and used to calculate renal vascular resistance

  2. Glomerular filtration rate

    Time frame: 4 months

    Measured by iohexol clearance

Secondary outcomes

  1. Arterial stiffness

    Time frame: 4 months

    Measured by SphygmoCor

  2. Insulin sensitivity

    Time frame: 4 months

    Measured by hyperinsulinemic-euglycemic clamp

Study contacts

Contact information is provided by the study sponsor or research team.

Kalie Tommerdahl, MD

CONTACT

[email protected]

(206) 616-9015

Sponsors and collaborators

Lead sponsor

Kalie Tommerdahl

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • University of Colorado, Denver

Registry information

Acronym: MANATEE-T1D

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Oct 4, 2021
Registry last updated
Jun 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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