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Intraportal or Intramuscular Site for Islets in Simultaneous Islet and Kidney Transplantation

Open Multi-Center Randomized Study to Compare Safety and Efficacy of Islet Transplantation Using The Intraportal or Intramuscular Site in Simultaneous Islet and Kidney Transplantation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01967186
Enrollment
36
Registered
2013-10-22
Start date
2007-04-30
Completion date
2016-07-31
Last updated
2015-10-06

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

Conditions

End Stage Renal Disease, Type 1 Diabetes

Keywords

Type 1 diabetes, islets, transplantation, nephropathy, intramuscular

Brief summary

Islet transplantation is a promising treatment of type 1 diabetes in selected cases. Results are however hampered by a relatively low number of islets surviving the transplantation into the liver, which currently is the site for transplantation. In the present study we compare a new transplantation site (intramuscular in the arm) to the golden standard (the liver) in patients undergoing kidney transplantation from the same donor. In half of the intramuscular transplanted patients, the islets will be mixed with mesenchymal stemcells from the recipient to, possibly, improve the immunological aspects of the transplantation.

Interventions

PROCEDUREIntraportal islet transplantation
PROCEDUREIntramuscular islet transplantation
PROCEDUREIntramuscular transpl with stemcells
PROCEDUREKidney transplantation

All patients will undergo kidney transplantation regardless of arm

Sponsors

The Nordic Network For Clinical Islet Transplantation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Male and female patients age 18 to 65 years of age. * Ability to provide written informed consent. * Mentally stable and able to comply with the procedures of the study protocol. * Clinical history compatible with type 1 diabetes with onset of disease at \< 40 years of age and insulin-dependence for \> 5 years at the time of enrolment. * Absence of stimulated C-peptide \<0.1 nmol/L in response to a MMTT. * All subjects must have received adequate medical treatment of their diabetes under the guidance from an experienced diabetologist. * All subjects must have renal failure and be eligible for renal transplantation according to local criteria.

Exclusion criteria

* Patients with prior organ transplants * Patients that qualify for local simultaneous pancreas-kidney transplantation program and who prefer that option * Patients with body mass index BMI \> 28. * Insulin requirement \> 1 Unit/kg/day. If the patient is on peritoneal dialysis the same limit is set when the extra carbohydrates in the dialysis fluids have been accounted for. * Consistently abnormal liver function tests ( \> 1.5 x the upper limit of normal on two consecutive measurements \> 2 weeks apart) * Unstable diabetic retinopathy * Hypercoagulability disorder or coagulopathy or International normalized ratio (INR)\>1.5 * Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin * Patients with unstable cardiovascular status * Patients with active infections, unless treatment is not judged necessary by the investigators * Patients with serological evidence of infection with HIV, hepatitis B (patients with serology consistent with previous vaccination and a history of vaccination are acceptable) or hepatitis C.

Design outcomes

Primary

MeasureTime frameDescription
C-peptide derived from the Mixed Meal Tolerance Test (MMTT)365 days (+/-14) after kidney transplantationPercentage of patients in each study group reaching a systemic C-peptide derived from the MMTT above 0.1 nmol/L basal (fasting) and 90-min 0.3 nmol/L 75 (+/-5) and 365 days (+/-14) after kidney transplantation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026