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OpenTrials
Completed

NCT Number: NCT00571818

The Prospective Evaluation of Pancreatic Function in Pancreas Transplant Recipients

The purpose of this study is to understand how the pancreas functions after transplantation and particularly why high blood sugar levels develop. It will also analyze the effect of the medicines used to prevent rejection on blood sugar levels.

The hypothesis to be tested is that hyperglycemia more than six months after successful pancreas transplant results from a defect in insulin secretion, insulin resistance, or both.

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Key information

Age range

19 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Nebraska Medical Center

Omaha, Nebraska, 68198, United States

About this study

Type I diabetes mellitus (DM1) is an autoimmune disease characterized by destruction of the insulin-secreting beta cells. Insulin replacement has been the cornerstone of therapy for patients with DM1. However, pancreas transplantation, utilizing the whole pancreas as a means to replace the destroyed beta cells, has become a therapeutic alternative. The goal of pancreas transplantation is the establishment of long-term euglycemia, thereby preventing or allowing for the repair of end-organ complications.

Maintenance of the pancreas allograft over many years remains the goal in following pancreas transplant recipients over time. The onset of hyperglycemia less than one year after transplant is usually due to issues of surgical technique or acute rejection. However, the onset of hyperglycemia after one year of pancreas transplant is more problematic because the underlying causes are less clear and have been less well characterized. Currently, there is no protocol for definitively identifying the causes of hyperglycemia in pancreas transplant recipients over one year. This project will systematically characterize beta cell function and peripheral tissue response to insulin in patients who have received an earlier successful pancreas transplant who have developed hyperglycemia.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Hyperglycemic pancreas transplant recipients:
  • ages 19-65
  • received a pancreas transplant ≥ 9 months previously
  • fasting glucose levels ≥ 126 mg/dl
  • hemoglobin A1C > 1% above normal
  • Euglycemic pancreas transplant recipients:
  • ages 19-65
  • received a pancreas transplant ≥ 9 months previously
  • fasting glucose levels are < 126 mg/dl
  • normal HbA1C without taking any medications for the treatment of high blood sugars.
  • Euglycemic Kidney Transplant Recipients:
  • ages 19-65
  • no prior diagnosis of diabetes
  • received a kidney transplant ≥ 9 months previously
  • showing continued function
  • Euglycemic Healthy Control Subjects:
  • ages 19-65
  • no diabetes or renal disease

Exclusion criteria

  • Hyperglycemic pancreas transplant recipients:
  • chronic illnesses that would decrease insulin sensitivity (
  • terminal illness
  • BMI > 30 kg/m2
  • serum creatinine > 2 mg/dl
  • hemoglobin < 10 g/dl
  • an episode of acute rejection with the preceding 3 months of entry.
  • Euglycemic pancreas transplant recipients:
  • Exclusion criteria are the same as with hyperglycemic transplant patients.
  • no diagnosis of type 2 diabetes.
  • Euglycemic Kidney Transplant Recipients:
  • Exclusion criteria are the same as for euglycemic pancreas transplant recipients above.
  • Euglycemic Healthy Control Subjects:
  • chronic illnesses
  • medications known to affect glucose metabolism
  • a history of smoking
  • serum creatinine ≥ 1.5 mg/dl
  • BMI > 30 kg/m2.

Treatment and study plan

Oral Glucose Tolerance Test

Procedure

test done over 2 hours

IV Glucose Tolerance Test

Procedure

Done over 4 hours

Primary outcomes

  1. Evaluate beta cell secretion

    Time frame: 9 months post-transplant or at time of participation for controls

    Evaluate beta cell secretion by oral glucose tolerance test (done over 2 hours) and IV Glucose Tolerance Test (done over 4 hours)

  2. Evaluate insulin sensitivity/glucose effectiveness

    Time frame: 9 months post-transplant or at time of participation for controls

    Evaluate insulin sensitivity/glucose effectiveness by oral glucose tolerance test (done over 2 hours) and IV Glucose Tolerance Test (done over 4 hours)

Sponsors and collaborators

Lead sponsor

University of Nebraska

Other

Registry information

Important dates

Study start
2000
Primary completion
2008
Study completion
2010
First posted
Dec 12, 2007
Registry last updated
Oct 10, 2023

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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