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Completed

NCT Number: NCT01186562

Sitagliptin Therapy to Improve Outcomes After Islet Autotransplant

The purpose of the study is to test the effects of sitagliptin on the need for insulin (the hormone that lowers blood sugars) by patients who receive a pancreatectomy and islet autotransplant for chronic pancreatitis.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Minnesota

Minneapolis, Minnesota, 55455, United States

About this study

At the current time, about one-third of patients are insulin independent (do not need to take insulin) after autotransplant, but the other two-thirds still need some insulin. Sitagliptin works by increasing the amount of a hormone called glucagon-like peptide 1, or GLP-1, in the body which then increases the amount of insulin that is made by the beta cells(the insulin producing cell of the islets). GLP-1 might also help protect beta cells from dying under stressful conditions and increase the production of new beta cells.

The primary goal of this study is to see if taking sitagliptin for one year after islet autotransplant increases the number of patients who achieve and maintain insulin independence. Other goals of this study are to see if sitagliptin reduces the amount of insulin injections needed or helps the islets make more insulin.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥18 years
  • Scheduled for total pancreatectomy and IAT at UM

Exclusion criteria

  • Pre-existing diabetes mellitus or hyperglycemia with fasting glucose ≥115 mg/dl
  • Medical conditions which, in the opinion of the investigator, might impact islet function (e.g asthma or inflammatory disease requiring chronic systemic corticosteroids)
  • Significant renal disease: serum creatinine levels of >3.0 mg/dL in men and >2.5 mg/dL in women, or end-stage renal disease requiring hemodialysis or peritoneal dialysis.
  • For female subjects, plans to become pregnant or unwillingness to practice birth control for 18 months.
  • Islet yield <1,000 IE/kg body weight (exclusion for treatment with drug/placebo)

Treatment and study plan

Sitagliptin

Drug

100 mg PO daily

Placebo

Drug

Placebo

Primary outcomes

  1. Insulin Independence

    Time frame: 12 months

    percentage of patients insulin independent

Secondary outcomes

  1. Insulin Independence

    Time frame: 18 months

    percentage of patients insulin independent

  2. Area Under the Curve (AUC) C-peptide (ng/dL*Min)

    Time frame: 12 months

    AUC C-peptide obtained from a mixed meal test (measured time 0 to 2 hours after Boost HP)

  3. AUC C-peptide

    Time frame: 18 months

    AUC C-peptide (ng/dL*min) from mixed meal tolerance test (measured times 0 to 2 hours after Boost HP)

  4. Acute C-peptide Response (ACR) to Glucose

    Time frame: 12 months

    Derived from intravenous gluocose tolerance testing (0 to 10 minute measures after dextrose bolus)

  5. Acute C-peptide Response (ACR) to Glucose

    Time frame: 18 months

    Derived from intravenous glucose tolerance test (0 to 10 minute measures after IV dextrose bolus)

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Registry information

Official study title

A Double-Blind, Randomized, Placebo Controlled Intervention Study to Assess the Impact of Sitagliptin 100 mg/Day for 1 Year on Insulin Independence Following Pancreatectomy and Autoislet Transplantation

Important dates

Study start
2010
Primary completion
2015
Study completion
2016
First posted
Aug 23, 2010
Registry last updated
May 31, 2017

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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