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:
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
  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:


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