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Primary outcome measurement is a parameter of functional beta cell mass at 6 months PT. Functional beta-cell mass will be calculated using the AUC/min between 150 and 160 min during hyperglycemic clamp at 180 mg/dl.
The investigators hypothesize that functional beta-cell mass will be more than 20% compared to healthy controls.
Secondary outcome measurements:
Functional beta-cell mass at 2,12,18,24,36,48 and 60 months PT.
The investigators will also compare at 2, 6,12, 24,36,48 and 60 months the changes against base-line (base-line = before first intraperitoneal transplantation):
Histopathology of a biopsy specimen of the human intraperitoneal beta cell implant, at time of the second implant. Comparison with composition of graft, identification of microenvironment of host origin and correlation with functional assessment will be performed.
Full description
In recipients with loss of long-term function after intraportal implantation (Group A)
To implant an alginate embedded human beta cell graft in a "therapeutic" dose in the intraperitoneal cavity of type 1 diabetic patients under immunosuppression with tacrolimus/MMF.
To obtain histopathology of a biopsy specimen of the intraperitoneal human beta cell implant.
To assess the safety profile, metabolic and immune effects of alginate embedded implants in the intraperitoneal cavity.
In patients that are candidates for islet cell transplantation (Group B)
To implant an alginate embedded human beta cell graft in a "therapeutic" dose in intraperitoneal cavity of type 1 diabetic patients under immunosuppression with tacrolimus/MMF.
To obtain histopathology of a biopsy specimen of the intraperitoneal human beta cell implant
To assess the safety profile, metabolic and immune effects of alginate embedded implants in the intraperitoneal cavity.
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Inclusion criteria
Group A:
Patients with loss of long-term function after intraportal implantation (- Patients with type 1 insulin-dependent diabetes who received two intraportal implantations > 12 months ago.
Group B:
Patients that are candidates for islet cell transplantation - age 18-65 years, male or female, Caucasian or not; only subjects < 50 yrs will be allocated to the rituximab treatment arm
body weight < 100 kg; patients with a bodyweight of < 80kg, will receive priority
patients with a BMI ≤ 27 kg/m2 will receive priority
Type 1 insulin-dependent diabetes
C-peptide < 0.07 nmol/l (< 0.2 µg/l) 6 min. after glucagon IV (1mg) (glycemia > 180 mg/dl)
Intensive insulin therapy for more than two years, patients with insulin pump during at least 2 months before inclusion will receive priority
Patients should have at least one of the following chronic complications of diabetes:
Cooperative and reliable patient giving informed consent by signature
Exclusion criteria
Women of reproductive age
Primary purpose
Allocation
Interventional model
Masking
10 participants in 2 patient groups
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Central trial contact
Bart Keymeulen, MD PhD; Robert Hilbrands, MD PhD
Data sourced from clinicaltrials.gov
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