Trial Comparing Metabolic Efficiency of Islet Graft to Intensive Insulin Therapy for Type 1 Diabetes's Treatment (TRIMECO)
This study is currently recruiting participants.
Verified October 2012 by University Hospital, Grenoble
Sponsor:
University Hospital, Grenoble
Information provided by (Responsible Party):
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT01148680
First received: June 21, 2010
Last updated: October 8, 2012
Last verified: October 2012
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Purpose
Efficacy of pancreatic islet transplantation at 6 months compared to an intensive insulin therapy for 2 categories of patients: patients with unstable diabetes and patients who underwent kidney transplantation.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetes Mellitus, Type 1 |
Procedure: human pancreatic islet transplantation |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Randomized Controlled Trial Comparing the Metabolic Efficiency of Allogeneic Pancreatic Islet Transplantation to Intensive Insulin Therapy for the Treatment of Type 1 Diabetes |
Resource links provided by NLM:
Genetics Home Reference related topics:
type 1 diabetes
MedlinePlus related topics:
Diabetes
Diabetes Medicines
Diabetes Type 1
Endocrine Diseases
Islet Cell Transplantation
Metabolic Disorders
U.S. FDA Resources
Further study details as provided by University Hospital, Grenoble:
Primary Outcome Measures:
- ß score evaluation 6 months after first infusion (group 1 'immediate registration on infusion waiting list') or 6 months after inclusion (group 2: 'delayed registration on infusion waiting list') [ Time Frame: 6 months after first infusion (group 1) or 6 months after inclusion (group 2) ] [ Designated as safety issue: No ]Metabolism evaluated by ß score. This score uses 4 intermediate scores ranging from 0 to 2 associated with the following 4 indicators: HbA1c, basal C peptide (or stimulated C-peptide), daily insulin dose (U/kg) or intake of oral antidiabetic drugs and fasting glycaemia. The total of the intermediate scores ranges from 0 to 8. Islet graft will be considered as successful if the ß score is equal to or greater than 6
Secondary Outcome Measures:
- Evaluation of metabolism indicators : ß-score and individual analysis of the 4 components of the ß-score [ Time Frame: 6 and 12 months ] [ Designated as safety issue: No ]Metabolism indicators at 6 and 12 months : ß-score (quantitative analysis by mean score comparison), individual analysis of the 4 components of the ß-score (HbA1c, basal C peptide (or stimulated C-peptide), daily insulin dose (U/kg) or intake of oral antidiabetic drugs and fasting glycaemia), lability index, ADRR score, Clarke score
- Measure of quality of life (SF36, DQOL, DHP) [ Time Frame: at inclusion time, at 6 months and at 12 months after first infusion (group 1) or after inclusion (group 2) ] [ Designated as safety issue: No ]Measure of quality of life (SF36, DQOL, DHP) for Group 1 ('immediate registration on infusion waiting list'): at inclusion time, at 6 months and at 12 months after first infusion For Group 2 ('delayed registration on infusion waiting list'): at inclusion time, 6 months after inclusion, at 6 months and at 12 months after first infusion
- Cost evaluation of islet cell infusion [ Time Frame: 6 months ] [ Designated as safety issue: No ]Cost comparison between islet cell infusion (group 1 'immediate registration on infusion waiting list')and intensive insulin therapy (group 2 'delayed registration on infusion waiting list') at 6 months, from a hospital perspective as well as a health-insurance system perspective
- Evaluation of side effects and iatrogenic effects [ Time Frame: at 6 months and 12 months after infusion ] [ Designated as safety issue: Yes ]Evaluation of side effects and iatrogenic effects at 6 months and 12 months after infusion
| Estimated Enrollment: | 40 |
| Study Start Date: | June 2010 |
| Estimated Study Completion Date: | December 2014 |
| Estimated Primary Completion Date: | June 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: immediate registration on infusion list
group 1 'immediate registration on infusion waiting list' : patients who will be immediately registrated on islet cell infusion waiting list after randomization
|
Procedure: human pancreatic islet transplantation
Iterative injection of pancreatic islets (minimum: 250,000 IEQ / injection or 3500 IEQ / kg / injection) with a threshold required total of 11,000 IEQ / kg in 2 or 3 injections per patient)
|
|
delayed registration on infusion list
group 2 'delayed registration on infusion waiting list' : patients who will be registrated 6 months later on islet cell infusion waiting list after randomization
|
Procedure: human pancreatic islet transplantation
Iterative injection of pancreatic islets (minimum: 250,000 IEQ / injection or 3500 IEQ / kg / injection) with a threshold required total of 11,000 IEQ / kg in 2 or 3 injections per patient)
|
Eligibility| Ages Eligible for Study: | 18 Years to 64 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patient with type 1 diabetes or C-peptide negative diabetes Diabetes duration > 5 years
- No residual insulin secretion (plasmatic basal and stimulated C-peptide < 0.3 ng/ml)
- HbA1c considered acceptable by the selection committee
- Insulin needs < 0.85 IU/kg/day
Islet cell infusion after kidney graft
- Patient with terminal renal failure and functional kidney graft for at least 6 months (creatinine clearance greater than or equal to 35 ml/min)
- Patient whose glycaemic control obtained with insulin therapy could threaten kidney graft survival and/or significantly alter quality of life. This situation is assessed by a diabetologist
Islet cell infusion only: patient with major glycaemic variability despite proper intensive insulin therapy, closely monitored by a diabetologist. Poor glucose control, assessed by a diabetologist, endangers the patient's life and/or significantly alters personal, social, professional and family quality of life. At least one of these criteria must be fulfilled :
- Hypoglycaemia unawareness, blood glucose level < 3mmol/L or 0.54 mg/L
- At least 2 severe hypoglycaemia events (defined by the necessity of a third party's assistance) per year or a ketoacidosis requiring patient's hospitalization during the last year.
- Impairment of quality of life or life-threat for patient or other persons, or progressive complications despite optimal insulin therapy
- Social Security membership or benefit from Social Welfare
Exclusion Criteria:
- Age< 18 and > 65
- Diabetes duration < 5 years
- Criteria specifically related to the islet intraportal injection procedure: hemostasis problem, haemoglobin level < 11g/dL for women and <12g/dL for men, abnormalities of complete blood count, documented liver pathology (alkaline phosphatases, gamma GT, transaminases levels over twice normal values) ; pancreatitis history, gallbladder stones that could potentially migrate; HLA hyperimmunisation (PRA >20%).
Criteria related to diabetes complications :
- Non-stabilized proliferating diabetic retinopathy
- Creatininaemia > 16 mg/dL
- Exclusion criteria non-specifically related to islet infusion: evolutive vascular disease, evolutive cardiopathy (especially myocardial infarction less than 6 months ago, cerebrovascular stroke less than 6 months ago, evolutive arteritis with trophic disorders) ; systemic infection including hepatitis C and HIV ; leuconeutropenia ; thrombocytopenia, non-stabilized neoplastic pathology ; pregnancy or project of pregnancy within the next 24 months ; poor therapeutic compliance
- Criteria related to immunosuppressive protocol : renal failure (glomerular filtration < 35 ml/min/1.73 m²) and/or proteinuria > 0.5 g/24h ; non-treated hyperlipidemia (LDL-C > 130 mg/dL) ; blood pressure > 160/100 mmHg
- Clinical insulin resistance : assessed by patient's weight, BMI and exogenous insulin requirements (BMI > 30 kg/m² or insulin dose > 0.85 UI/kg/day)
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01148680
Contacts
| Contact: Jean-Luc Bosson, MD | +33476769260 | JLBosson@chu-grenoble.fr |
| Contact: Myriam Haddouche | +33476765040 | MHaddouche@chu-grenoble.fr |
Locations
| France | |
| University Hospital, Department of Endocrinology | Recruiting |
| Strasbourg, Alsace, France, 67000 | |
| Contact: Laurence Kessler, Pr +33 3 88 11 62 67 Laurence.Kessler@medecine.u-strasbg.fr | |
| Principal Investigator: Laurence Kessler, Pr | |
| Sub-Investigator: François Moreau, MD | |
| University Hospital Gabriel Montpied, Department of Endocrinology | Not yet recruiting |
| Clermont Ferrand, Auvergne, France, 63003 | |
| Contact: Igor Tauveron, Pr +33 4 73 751 529 itauveron@chu-clermontferrand.fr | |
| Principal Investigator: Igor Tauveron, Pr | |
| Sub-Investigator: Beatrice Roche, MD | |
| University Hospital | Recruiting |
| Besançon, Franche-Comté, France, 25000 | |
| Contact: Alfred PENFORNIS, Pr +33 3 81 66 81 92 alfred.penfornis@univ-fcomte.fr | |
| Principal Investigator: Alfred Penfornis, Pr | |
| University Hospital, Department of Endocrinology | Recruiting |
| Montpellier, Languedoc-Roussillon, France, 34000 | |
| Contact: Anne Wojtusciszyn, MD +33 4 67 33 83 82 a-wojtusciszyn@chu-montpellier.fr | |
| Principal Investigator: Anne Wojtusciszyn, MD | |
| Sub-Investigator: Eric Renard, Pr | |
| University Hospital, Department of Endocrinology | Recruiting |
| Nancy, Lorraine, France, 54000 | |
| Contact: Bruno Guerci, Pr +33 3 83 65 65 28 b.guerci@chu-nancy.fr | |
| Principal Investigator: Bruno Guerci, Pr | |
| Sub-Investigator: Luc Frimat, Pr | |
| University Hospital, Department of General Surgery and Endocrinology | Recruiting |
| Lille, Nord Pas de Calais, France, 59000 | |
| Contact: Marie-Christine Vantyghem, MD +33 3 20 44 43 32 Marie-Christine.VANTYGHEM@CHRU-LILLE.FR | |
| Principal Investigator: Marie-Christine Vantyghem, MD | |
| Sub-Investigator: François Pattou, Pr | |
| Sub-Investigator: Violetta Raverdy, MD | |
| Sub-Investigator: Christian Noel, Pr | |
| University Hospital, Department of Endocrinology | Recruiting |
| Grenoble, Rhône-Alpes, France, 38000 | |
| Contact: Pierre-Yves Benhamou, Pr + 33 476769349 PYBenhamou@chu-grenoble.fr | |
| Principal Investigator: Pierre-Yves Benhamou, Pr | |
| Sub-Investigator: François Bayle, MD | |
| HCL Sud, Department of Endocrinology | Recruiting |
| Lyon, Rhône-Alpes, France, 69000 | |
| Contact: Charles Thivolt, Pr +33 4 78 86 14 87 charles.thivolet@chu-lyon.fr | |
| Principal Investigator: Charles Thivolet, Pr | |
| Sub-Investigator: Emmanuel Morelon, Pr | |
| Sub-Investigator: Lionel Badet, Pr | |
| Switzerland | |
| Hopitaux Universitaires de Genève | Not yet recruiting |
| Geneve, Switzerland, CH-1211 | |
| Contact: Thierry Berney, Pr +41 22 37 23 404 Thierry.Berney@hcuge.ch | |
| Principal Investigator: Thierry Berney, Pr | |
| Sub-Investigator: Christian Toso, MD | |
Sponsors and Collaborators
University Hospital, Grenoble
Investigators
| Principal Investigator: | Pierre-Yves Benhamou, Pr | University Hospital, Grenoble |
More Information
Publications:
| Responsible Party: | University Hospital, Grenoble |
| ClinicalTrials.gov Identifier: | NCT01148680 History of Changes |
| Other Study ID Numbers: | DCIC 08 31 |
| Study First Received: | June 21, 2010 |
| Last Updated: | October 8, 2012 |
| Health Authority: | France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) |
Keywords provided by University Hospital, Grenoble:
|
Islet Cell Transplantation Metabolic Diseases Endocrine System Diseases |
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 19, 2013