Diabetes Mellitus, Type 1 Clinical Trial
Official title:
UVA Islet Cell Transplantation in Patients With Type I Diabetes
Verified date | February 2009 |
Source | University of Virginia |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
This protocol will provide islet cell transplantation to two separate populations in need of
a pancreas transplant:
Group I: Islet Cell Transplantation in Type I Diabetics without Kidney Problems
Group II: Islet Cell Transplantation in Type I Diabetics Who Have a Stable Functioning
Kidney Transplant
The targeted patients have very brittle diabetes or dangerous hypoglycemic unawareness and
may benefit from transplantation over continuing insulin therapy, even though chronic
immunosuppression is required. We believe that in these patients, the islet transplant
procedure promises enough potential benefit to justify subjecting patients who have not
previously had a transplant to the risk of immunosuppression.
In patients who are already subject to the dangers of chronic immunosuppression for other
reasons, i.e. to prevent rejection of a kidney allograft, the islet transplantation
procedure itself is the principal additional risk and this risk should be minimal. In these
patients (our Group II), the potential benefit from improved glycemic control is that it
promises to slow or even reverse diabetic complications, such as vascular problems leading
to kidney damage. It is this rationale that has made pancreas transplantation a widely
accepted option in patients with renal failure, despite the risks associated with whole
pancreas transplantation. Islet cell transplantation aims to provide a potentially lower
risk procedure that has similar relief from diabetic complications.
Status | Active, not recruiting |
Enrollment | 20 |
Est. completion date | January 2012 |
Est. primary completion date | January 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Type I Diabetes Mellitus for at least 5 years - Unstable control of diabetes despite intensive care by an endocrinologist, including episodes of dangerously low blood sugars - Group I must have healthy kidneys - Group II (islet after kidney) must have a stable kidney allograft for at least 6 months Exclusion Criteria: - Unstable diabetic eye disease - Poor kidney function - Type II Diabetes as determined by blood tests - Any history of cancer, except certain skin cancers - Pregnant or unwilling to use adequate birth control - Very high hemoglobin A1c levels - Poor control of blood pressure, despite use of medications - Very high insulin requirements - History of exposure to HIV - Active Hepatitis B or Hepatitis C infection |
Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | University of Virginia | Charlottesville | Virginia |
Lead Sponsor | Collaborator |
---|---|
University of Virginia | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Wyeth is now a wholly owned subsidiary of Pfizer |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | A decrease in the average daily insulin requirement post-islet cell transplantation. | Post-transplant | No |
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