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Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation

Phase 2 Study of Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation With Steroid Free Immunosuppression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01123187
Enrollment
14
Registered
2010-05-14
Start date
2003-03-31
Completion date
2016-04-30
Last updated
2025-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes, Organ Transplantation, Immunosuppression

Keywords

diabetes type 1, kidney transplantation, islet, hypoglycemia

Brief summary

This single center phase 2 clinical trial, is designed for confirming the efficacy and safety of sequential islet allotransplantation with steroid free immunosuppression in patients with previous kidney transplantation.

Detailed description

The beneficial effects of glycemic control on both survival and function of transplanted kidneys in patients with type 1 diabetes mellitus have been recognized. 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. The study primary efficacy endpoint is graft survival defined as insulin independence and HbA1c \< 8% at 1 year post first transplant. Secondary outcomes are graft function and metabolic control The immunosuppression protocol for the kidney graft was converted to sirolimus+tacrolimus regimen 6 months before islet transplantation to exclude negative effects on kidney graft function.

Interventions

Islet transplantation consisted of up to three sequential fresh islet infusions within three months. Access to the portal vein was gained under general anesthesia by percutaneous catheterisation of a peripheral portal branch under ultrasound guidance or by surgical catheterisation of a small mesenteric vein.

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
University Hospital, Lille
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Islet transplantation

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Type 1 diabetes mellitus. Documentation of negative basal and stimulated C-peptide and diagnosis of diabetes for at least 5 years. * Recipient of renal transplant with good function (creatinine clearance \>/=60 ml/min) * Stable immunosuppression consisting of any combination of sirolimus, tacrolimus for at least 6 months, without major complications * Ability to give informed consent. * Age greater than or equal to 18 years or less than or equal to 65 years * No evidence of liver disease (liver enzymes \< twice the upper limit of normal)

Exclusion criteria

* Age below 18 years and above 65 years * Significant cardiovascular disease, including non-correctable coronary artery disease and/or recent myocardial infarction(within last 12 months); extensive peripheral vascular disease not correctable by surgery, unstable angina * Untreated proliferative retinopathy. * Recent Cerebrovascular accident (within last 12 months) * Recent unresolved acute infection, or chronic infection, including tuberculosis, HIV, HBV, HCV, CMV or positive skin test for TB * Any history of malignancy, except squamous or basal skin cancer or in situ cancer of the cervix. * History of non-compliance, or inability to demonstrate capacity to comply with strict blood glycemic control and insulin pump therapy. * Psychiatric illness that is untreated, or likely to interfere significantly with transplantation despite treatment. * Pregnant women, women intending future pregnancy, women of reproductive potential who are unable or unwilling to follow effective contraceptive measures for the duration of immunosuppressive therapy * Fasting C-peptide \> 0.2 ng/ml * Creatinine \> 25mg/l * Alkaline phosphatase, total bilirubin, Alanine Aminotransferase (ALT)or Aspartate Aminotransferase (AST) \> twice the upper limit of normal * Significant liver disease (elevation of liver enzymes \> twice the upper limit of normal for each of ALT and AST, liver masses including portal vein thrombosis, evidence of portal hypertension, or significant, untreated gallbladder disease (i.e., gallstones).

Design outcomes

Primary

MeasureTime frameDescription
Composite criteria: insulin independence and Glycosylated Hemoglobin (HbA1c) under 8% at one year after the transplantationOne yearPercent of insulin-independent patients with a Glycosylated Hemoglobin (HbA1c) under 8% at one year after injection of approximately 10,000 islets equivalents / kg (IE/kg).

Secondary

MeasureTime frameDescription
The number of adverse events1 yearThe number of adverse events related to the procedure and to the immunosuppression
Number of severe episodes of hypoglycemia1 yearNumber of severe episodes of hypoglycemia (requiring the use of third)
Evaluation of Diabetes complications1 yearEvaluation of Diabetes complications: retinopathy, neuropathy, nephropathy
Lipid metabolism1 yearLipid metabolism assessed by measurement of total cholesterol and HDL cholesterol, triglycerides, ApoA1, apoB, apoE, free fatty acids and lipid.
Evaluation of kidney function1 yearEvaluation of kidney function (creatinine, creatinine clearance,proteinurie)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026