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Completed

NCT Number: NCT01232946

Cooperation of Insulin and GLP-1 on Myocardial Glucose Uptake

27 Type 2 diabetic subjects (HbA1c 7.5 - 9.5%) currently treated with diet and exercise alone or with oral antidiabetic agents will be randomly assigned to one of three treatment groups: insulin detemir, liraglutide, or liraglutide plus detemir (9 subjects per group), on a background of metformin 2000 mg per day. After 3 months' treatment, PET measurements of myocardial fuel selection will take place, under fasting conditions in the morning following that day's treatment injection(s).

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Indiana Clinical Research Center

Indianapolis, Indiana, 46202, United States

About this study

The investigators will test the hypothesis that effects of liraglutide plus insulin detemir on myocardial fuel selection will be greater than the effects of either agent alone. 27 Type 2 diabetic subjects (HbA1c 7.5 - 9.5%) currently treated with diet and exercise alone or with oral antidiabetic agents will be randomly assigned to one of three treatment groups: insulin detemir, liraglutide, or liraglutide plus detemir (9 subjects per group). All subjects will undergo an initial standardization of background treatment to metformin 2000 mg per day, followed by randomized assignment to 3 months' treatment with liraglutide 1.8 mg/day (once daily each morning, tapering up according to label instructions) and/or detemir (administered twice daily, initially at 10 units per day then titrated to achieve fasting morning glucose readings below 130 mg/dL). PET measurements of myocardial fuel selection will take place at the end of this treatment period, under fasting conditions in the morning following that day's treatment injection(s).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Type 2 diabetic
  • 18-50 years
  • BMI > 25kg/m2
  • HbA1c 7.0-10.0%
  • Treated with up to 2 oral agents

Exclusion criteria

  • Chronic illness or infection (other than diabetes mellitus)
  • Known coronary artery disease, structural heart disease or abnormal ECG on screen.
  • Treatment with >2 antihypertensive agents or blood pressure >140/95 on two occasions during screening
  • History of claustrophobia, musculoskeletal or other factors which would result in an inability to comfortably remain within the PET scanner gantry for the duration of the imaging protocol.
  • Occupational, investigational or other known radiation exposure which together with the planned radiologic studies, will result in greater than 500 mrem total exposure in a 12 month period.
  • Current pregnancy
  • Treatment with GLP-1 agonist or DPP4 inhibitor within the past 6 months
  • Known intolerance to GLP-1 agonist
  • Personal history of pancreatitis, personal or family history of medullary thyroid carcinoma, or other contraindications to liraglutide treatment.
  • Recognized microvascular complications (neuropathy, nephropathy, retinopathy).

Treatment and study plan

liraglutide

Drug

1.8mg subcutaneous qd for 3 months

Other names: Victoza

insulin detemir

Drug

5units subcutaneous bid titrated to fasting glucose of <130mg/dL for 3 months

Other names: Levemir

liraglutide plus insulin detemir

Drug

liraglutide 1.8mg subq qd plus insulin detemir 5units bid titrated to fasting blood glucose <130mg/dL for 3 months.

Other names: Vyctoza plus Levemir

Primary outcomes

  1. Myocardial Glucose Uptake

    Time frame: 3 months

    PET measurements of myocardial glucose uptake will be done after 3 months of exposure to liraglutide, insulin detemir, or liraglutide plus insulin detemir

  2. Myocardial Fatty Acid Oxidation Rate

    Time frame: 3 months

    PET measurements of myocardial glucose uptake will be done after 3 months of exposure to liraglutide, insulin detemir, or liraglutide plus insulin detemir

  3. Myocardial Fatty Acid Esterification Rate

    Time frame: 3 months

    PET measurements of myocardial glucose uptake will be done after 3 months of exposure to liraglutide, insulin detemir, or liraglutide plus insulin detemir

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Collaborators

  • Novo Nordisk A/S

Registry information

Important dates

Study start
2012
Primary completion
2017
Study completion
2017
First posted
Nov 2, 2010
Registry last updated
Aug 7, 2019

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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