Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation
The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2011 by University of Miami.
Recruitment status was Active, not recruiting
Recruitment status was Active, not recruiting
Sponsor:
University of Miami
Collaborators:
Health Resources and Services Administration (HRSA)
Information provided by:
University of Miami
ClinicalTrials.gov Identifier:
NCT00315588
First received: April 14, 2006
Last updated: August 4, 2011
Last verified: May 2011
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Purpose
The purpose of this study is to reverse hyperglycemia and insulin dependency, by islet cell transplantation, in patients with type 1 diabetes mellitus who have a stable kidney allograft.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetes Mellitus, Type 1 |
Procedure: Islet Transplantation |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation |
Resource links provided by NLM:
Genetics Home Reference related topics:
type 1 diabetes
MedlinePlus related topics:
Diabetes
Diabetes Medicines
Diabetes Type 1
Islet Cell Transplantation
Kidney Transplantation
U.S. FDA Resources
Further study details as provided by University of Miami:
Primary Outcome Measures:
- The endpoint of this clinical trial will be the functional capability of the islet allograft to normalize glucose metabolism in the absence of insulin therapy.
Secondary Outcome Measures:
- Partial graft function, as evidenced by basal C-peptide greater than 0.5 ng/ml
- Reduction in insulin requirements in those patients who do not achieve insulin independence
- Improvement in metabolic control as evidenced by improvement in: hemoglobin A1c [HbA1c] (should be < 6.5%), mean amplitude of glycemic excursions (MAGE), mean glucose meter readings, CGMS (continuous glucose monitoring system)
- Elimination or reduction in the incidence of hypoglycemic coma or unawareness
- Improvement in or decreased progression of microvascular, macrovascular, and neuropathic complications of diabetes
- Assessment of EXN to re-establish insulin independence or increase insulin secretion
| Estimated Enrollment: | 20 |
| Study Start Date: | December 2000 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
Intervention Details:
Detailed Description:
-
Procedure: Islet Transplantation
Islet transplantation
- To reverse hyperglycemia and insulin dependency by islet cell transplantation, in patients with Type 1 Diabetes Mellitus who have a stable kidney allograft;
- To eliminate the incidence of hypoglycemic coma and unawareness by islet cell transplantation;
- To assess long-term function of successful islet cell transplants;
- To determine whether the natural history of the microvascular, macrovascular and neuropathic complications of Diabetes Mellitus are altered following successful transplantation of islet cells.
- To assess the effect of exenatide to improve islet graft function and survival in subjects that demonstrate partial graft loss and have returned to using exogenous insulin.
- To assess the ability of exenatide to improve islet survival at time of islet transplantation
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patients between 18 and 60 years of age.
- Patients with type 1 diabetes mellitus.
- Patients with a renal transplant that is more than 6 months old.
- Patients with stable renal graft function for the preceding 6 months, i.e. no episodes of rejection and changes in serum creatinine no more than 0.5 mg/dl from baseline.
- Patients who are taking tacrolimus, sirolimus +/- steroids for maintenance immunosuppression for at least 6 months and are tolerating levels satisfactory for islet transplantation without severe complications.
- Patients with a body mass index (BMI) of less than or equal to 26.
Exclusion Criteria:
- Stimulated or basal C-peptide > 0.3 ng/ml.
- Patients with unstable renal function - serum creatinine greater than 0.5 mg/dl above baseline.
- Patients with proteinuria (albuminuria > 300 mg in 24 hours +/- protein) of new onset since kidney transplantation. If proteinuria or albuminuria is thought to originate from the native kidney(s) this will not be an exclusion criterion.
- Patients with corrected creatinine clearance of less than 40.
- Patients weighing more than 80 kg.
- Patients with a body mass index (BMI) of greater than 26.
- Insulin requirement > 1.0 U/kg/d.
- Anemia (hemoglobin: males < 11.0 g/dl; females < 10.0 g/dl).
- Abnormal liver function tests (consistently > 1.5 x normal range).
- Unstable diabetic retinopathy.
- Evidence of acute or chronic active Epstein-Barr virus (EBV) infection (IgM ≥ IgG). Patients will be eligible if serological testing becomes consistent with previous exposure (i.e. IgG > IgM).
- Patients with history of malignancy or current malignancy other than non-melanomatous skin cancer, or finding of any lesions or symptoms during screening that are suspicious for malignancy, until properly investigated and ruled out.
- Patients with elevation of prostate-specific antigen > 4 unless malignancy has been excluded.
- Patients with unstable cardiovascular status.
- Patients with active infections until adequately treated, unless treatment is not judged as necessary by the investigators (including, but not limited to, mild skin and nail fungal infections).
- Patients with serological evidence of infection with HIV, human t cell lymphotropic virus 1 (HTLV 1), HTLV 2, or hepatitis B (patients with serology consistent with previous vaccination and a history of vaccination are acceptable).
- Patients with history and/or serological evidence of hepatitis C (those patients with hepatitis C, already transplanted in this protocol will continue in this trial).
- Positive tuberculin test (unless proof of adequate treatment for latent tuberculosis can be provided).
- Patients with active peptic ulcer disease, gallstones, hepatic hemangioma, or portal hypertension.
- Patients who are pregnant or breastfeeding, or who intend to procreate.
Patients who are sexually active females who are not:
- post-menopausal,
- surgically sterile, or
- using an acceptable method of contraception (oral contraceptives, Norplant, Depo-Provera, and barrier devices combined with spermicidal gel are acceptable; condoms used alone are not acceptable).
- Active alcohol or substance abuse; smoking in the last 6 months.
- Patients with evidence of sensitization, i.e. panel reactive antibody (PRA) testing greater than 20%.
- Lack of updated immunizations per current Centers for Disease Control (CDC) guidelines, as well as immunization against hepatitis B, pneumococcus, and influenza (during season), unless medically contraindicated.
- Patients with psychogenic factors, which are judged at psychological evaluation, which make it unsafe to undergo islet transplantation, or which preclude therapeutic compliance.
- Patients with any condition or any circumstance that would make it unsafe to undergo an islet transplant.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00315588
Locations
| United States, Florida | |
| Diabetes Research Institute | |
| Miami, Florida, United States, 33136 | |
Sponsors and Collaborators
University of Miami
Health Resources and Services Administration (HRSA)
Investigators
| Principal Investigator: | Rodolfo Alejandro, M.D. | University of Miami |
More Information
Additional Information:
No publications provided by University of Miami
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Rodolfo Alejandro, MD, Diabetes Research Institute, University of Miami |
| ClinicalTrials.gov Identifier: | NCT00315588 History of Changes |
| Other Study ID Numbers: | 2000/0329 |
| Study First Received: | April 14, 2006 |
| Last Updated: | August 4, 2011 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by University of Miami:
|
Islet Transplantation |
Additional relevant MeSH terms:
|
Diabetes Mellitus Diabetes Mellitus, Type 1 Glucose Metabolism Disorders Metabolic Diseases |
Endocrine System Diseases Autoimmune Diseases Immune System Diseases |
ClinicalTrials.gov processed this record on May 23, 2013