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OpenTrials
Completed

NCT Number: NCT00568620

The Role of the Duodenum in the Pathogenesis of Insulin Resistance and Type 2 Diabetes Mellitus

In parallel with the increasing prevalence of obesity worldwide, type 2 diabetes mellitus (T2DM) has reached epidemic proportions. Despite a multitude of available therapies, only bariatric surgery (e.g., roux-en-Y gastric bypass (GBP)) has proven to be an effective long term treatment modality for morbid obesity. Moreover, the majority of T2DM patients who undergo GBP experience normalization of their blood glucose and are able to discontinue their anti-diabetes medications soon after the procedure. The insulin resistant state commonly seen in non-diabetic obese subjects also improves after GBP. Evidence from recent animal studies suggests that the rapid return to euglycemia seen in T2DM patients after GBP might in part result from excluding the duodenum from the flow of nutrients. With the use of enteral feeding tubes, we hope to better understand the factors in the human gut that may predispose obese individuals to the development of insulin resistance and T2DM.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Inclusion criteria

for lean, healthy control subjects:

  • Fasting plasma glucose (FPG) < 100
  • Age 18 to 55
  • BMI 18.5 to 24.9 kg/m2
  • Stable weight for prior 3 months

Inclusion criteria

for prediabetic individuals:

  • Based on American Diabetes Association criteria of FPG > 100 and <126
  • Age 18 to 55
  • BMI 35 to 60 kg/m2
  • Stable weight for prior 3 months

Inclusion criteria

for diabetic individuals:

  • Diagnosis of type 2 diabetes mellitus (T2DM) for < 5 years
  • Hemoglobin A1c < 8%
  • Age 18 to 55
  • BMI 35 to 60 kg/m2
  • Stable weight for prior 3 months

Exclusion criteria

Exclusion criteria

for all study subjects:

  • Use of any of the following medications: Thiazolidinediones, dipeptidyl-peptidase IV (DPP-IV) inhibitors (e.g., sitagliptin), GLP-1 analogs (e.g., exenatide).
  • Subjects with T2DM who are unable to maintain adequate glycemic control (i.e., having a fasting blood glucose that exceeds 250mg/dL on two consecutive tests) while temporarily discontinuing their oral diabetes medications for the study and in whom the study physician determines insulin therapy would not be appropriate.
  • Females with a positive pregnancy test
  • Prior gastric, duodenal, proximal jejunal surgery or pancreas resection 6. Known malabsorptive disorder 7. History of cancer in past 5 years 8. Renal insufficiency defined by serum creatinine > 1.5 mg/dl 9. Hepatic enzyme elevations of greater than twice the upper limits of normal 10. Current use of warfarin or clopidogrel 11. Intercurrent infections 12. Contraindication to nasogastric or nasojejunal feeding tube (e.g., deviated nasal septum, prior upper gastrointestinal bleed, or history of easy bleeding) 13. Residence outside the greater Nashville, TN area

Treatment and study plan

Placement of nasogastric feeding tube

Procedure

Glucose tolerance test via nasogastric feeding tube

50 g glucose tolerance test on day 1; 50 g glucose tolerance test with 30 mL oil on day 2; Intravenous glucose tolerance test on day 3

Nasojejunal feeding tube

Procedure

Glucose tolerance test via nasojejunal feeding tube

50 g glucose tolerance test on day 1; 50 g glucose tolerance test with 30 mL oil on day 2; Intravenous glucose tolerance test on day 3

Primary outcomes

  1. Insulin sensitivity

    Time frame: 3 days

Secondary outcomes

  1. Incretin effect

    Time frame: 3 days

Sponsors and collaborators

Lead sponsor

Vanderbilt University

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Important dates

Study start
2008
Primary completion
2012
Study completion
2016
First posted
Dec 6, 2007
Registry last updated
Nov 1, 2016

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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