Diabetes Mellitus, Type I Clinical Trial
Official title:
Islet Transplantation in Type 1 Diabetic Kidney Allograft Recipients
Verified date | October 2017 |
Source | Massachusetts General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study is to learn if islet transplantation is an effective treatment for
Type 1 diabetes in people who have had a kidney transplant.
The primary objectives of the study are:
- To set up islet transplantation in patients who have had a kidney transplant and who are
using an immunosuppressive regimen that works
The Secondary objective of the study is:
- To find out if successful islet transplantation leads to improved metabolic control and
reduced renal complication from diabetes
Status | Completed |
Enrollment | 7 |
Est. completion date | August 2016 |
Est. primary completion date | August 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Male and female subjects - Age 18 to 70 years of age - Have insulin dependent Diabetes Mellitus Type 1 - Are post-renal transplant on maintenance immunosuppression with stable renal function - HbA1c > 7.5% or < 7.5% and hypoglycemia unawareness Exclusion Criteria: - Weight more than 90 kg - Insulin requirement > 60 Units/day - Other (non-kidney) organ transplants except prior failed pancreatic graft. - Untreated or unstable proliferative diabetic retinopathy - Presence of de novo antibody production since the renal allograft or either Class I or Class II panel-reactive anti-HLA antibodies - Active infection - Negative screen for Epstein-Barr virus (EBV) - Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin - History of Factor V Leiden mutation - Any coagulopathy or medical condition requiring long-term anticoagulant therapy (e.g. warfarin) after transplantation (low-dose aspirin treatment is allowed) or subjects with international normalized ratio (INR) > 1.5 - Severe co-existing cardiac disease - Persistent elevation of liver function tests at the time of study entry - Acute or chronic pancreatitis - Male subjects with elevation of prostate specific antigen - Pregnancy - Positive screen for polyoma (BK) virus - Untreated hyperlipidemia - Recent hemorrhagic stroke - Factors associated with an increased risk of bleeding Contact PI for complete Incl-Excl criteria list. |
Country | Name | City | State |
---|---|---|---|
United States | Massachusetts General Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital | Boston Area Diabetes Endocrinology Research Center (funded by NIDDK) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Insulin Independence With Both an HbA1c = 6.5% and no Severe Hypoglycemic Events at 1 Year After the First Islet Transplant or a Reduction in HbA1c of at Least 1 Point and no Severe Hypoglycemic Events at 1 Year After the First Islet Transplant. | 1 year after the subject's first islet transplant | ||
Secondary | Number of Participants With a Decrease in HbA1c | Subjects will have a decrease in HbA1c of at least >1% | 1 year after subject's first islet transplant | |
Secondary | Stable or Decrease in Urinary Albumin and Creatinine Ratio and Serum Creatinine | Proteinuria and serum creatinine will be stable or decreased as compared to pre-transplant values | 1 year after subjects initial islet transplant | |
Secondary | An Absence Cardiovascular Events, Cerebral Vascular Accident, and Myocardial Infarction | 1 year after the subject's first islet transplant | ||
Secondary | Impact on Vision | Improvement of frequency of interventions and from changes in reported visual acuity with optical refraction and severity of diabetic retinopathy | 1 year after the subject's first islet transplant | |
Secondary | Absence of Negative Renal Impact Measures | Loss of allograft survivial (return to dialysis, retransplant, death) and Renal allograft function meausred by SCr | 1 year after the subject's first islet transplant | |
Secondary | Improvement of Metabolic Control | Whether there is an improvement in metabolic control in IAK will be evaluated based on improvement in basal c-peptide levels, MMTT, insulin requirements, and c-peptide to glucose, creatinine ratio (CPGCR). |
1 year after the subject's first islet transplant | |
Secondary | Number of Participants With a Decrease of Severe Hypoglycemic Events | Subjects will have a decrease in severe hypoglycemic events | 1 year after subject's first transplant | |
Secondary | Reduction of Insulin Requriements | Evidence of partial success will be considered for subjects who have a reduction in insulin requirements but who are not insulin independent. This will be assessed by comparing the pre-transplant insulin requirement expressed as insulin units per kg per day with the requirement preceding subsequent islet transplants and the insulin requirements at 6 months and 1, 2, and 3 years after the first and last transplant. | 1 year after the subject's first islet transplant |
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