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Completed

NCT Number: NCT00656864

Pioglitazone Incretin Study

Incretin hormones are hormones produced by the gut in response to food intake. These hormones help the body to control the metabolism of glucose (sugar). In particular, two incretin hormones (GLP-1 and GIP) cause the pancreas to secrete more insulin in response to high blood glucose levels. This helps the body to metabolize the glucose more effectively, lowering blood sugar levels. GLP-1 and GIP do not work as well in patients with type 2 diabetes (T2DM) as in subjects who do not have diabetes. This study tests whether a medicine called pioglitazone (Actos), which is commonly used to treat T2DM, improves the ability of GIP to increase insulin secretion.

To address this question the investigators will recruit patients with T2DM whose diabetes is controlled with either diet and exercise or with metformin (another medicine commonly used to treat T2DM). Subjects will undergo measurement of body fat by DEXA scanning and a series of studies to characterize their metabolism. These studies include an oral glucose tolerance test (a test sometimes used to diagnose diabetes), a mixed-meal challenge (to measure how much GLP-1 and GIP are produced in response to a meal) and measurement of insulin secretion in response to glucose and GIP given through a vein. The investigators will also obtain small samples of fat (from just under the skin of the belly) using a needle to measure levels of the receptor for GIP. Subjects will then be randomly assigned to 12 weeks of treatment with either pioglitazone or matching placebo (an inactive tablet that does not contain medication). The dose of pioglitazone will be increased during the first 4 weeks to the maximum prescribed dose of 45 mg per day. Subjects will be seen every 2-4 weeks during the treatment phase of the study. After 12 weeks of treatment all studies performed at the beginning of the study will be repeated. The pioglitazone treatment will continue until the end of testing, approximately 4 weeks.

The results of this study may give us information about why glucose control deteriorates in T2DM. This information might also lead to new ways to prevent or treat T2DM.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Vermont

South Burlington, Vermont, 05403, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Type 2 diabetes controlled with diet+exercise or metformin monotherapy
  • HbA1c less than or equal to 7%
  • Women will be non-fertile or practicing birth control

Exclusion criteria

  • Acute or chronic medical conditions that would contraindicate participation
  • Class III or IV heart failure
  • Pregnant or nursing women
  • Patients taking antidiabetic medications other than metformin, oral or chronic topical steroids, weight loss agents, antipsychotics, or other drugs that could affect insulin sensitivity or secretion.
  • AST or ALT more than 2.5 times the upper limit of normal
  • Active alcohol or drug abuse
  • Weight greater than 300 pounds

Treatment and study plan

pioglitazone

Drug

Starting dose at 15 mg for two weeks, then titrated up to 45 mg in the subsequent 2 weeks.

Other names: Actos (brand name for pioglitazone)

Placebo

Drug

placebo

Primary outcomes

  1. Change in incretin-mediated insulin secretion and receptor regulation of glucose-dependent insulinotropic peptide (GIP) in patients with type 2 diabetes.

    Time frame: 12 weeks per subject

Secondary outcomes

  1. Change in active GIP in response to an oral glucose tolerance test and mixed meal challenge

    Time frame: 12 weeks

  2. Change in active GLP-1 in response to the oral glucose tolerance test and the mixed meal challenge

    Time frame: 12 weeks

  3. Change in glucose response during the oral glucose tolerance test and mixed meal challenge

    Time frame: 12 weeks

  4. Change in insulin secretion during the oral glucose tolerance test and the mixed meal challenge

    Time frame: 12 weeks

  5. Change in the acute insulin response to glucose, insulin sensitivity and the disposition index during the IV glucose tolerance test.

    Time frame: 12 weeks

  6. Change in adipocyte GIP receptor mRNA expression levels.

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

University of Vermont

Other

Collaborators

  • Takeda

Registry information

Official study title

Effects of Pioglitazone on the Regulation of Insulin Secretion in Patients With Type 2 Diabetes

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Apr 11, 2008
Registry last updated
Feb 2, 2011

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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