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Islet Cell Transplantation Alone and CD34+ Enriched Bone Marrow Cell Infusion in Patients With Diabetes Mellitus: Steroid-Free Regimen

Primary Purpose

Type 1 Diabetes Mellitus

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Islet Cell Transplantation
Sponsored by
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring Type I Diabetes Mellitus, Immunosuppression, Islet Cell Transplant, Percutaneous Transhepatic Portal

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Candidates must be between the ages of 18 and 50. Candidates must have had insulin-dependent diabetes mellitus (IDDM) for at least 5 years and been under physician care for at least 6 months prior to enrollment in trial. Eligible candidates will have poorly controlled IDDM and manifest signs and symptoms severe enough to be incapacitating. These symptoms can include episodes of hypoglycemic unawareness (failure to recognize blood glucose levels < 54 mg/dl) or episodes requiring the assistance of others. Candidates may have poor diabetes control despite intensive insulin therapy (HbA1c > 8.0%). Creatinine clearance should be > 60 ml/min) Body Mass Index should be less than 26 Women of child-bearing age must have a negative pregnancy test and agree to follow effective contraceptive measures for the duration of the trial. Exclusion Criteria: Previous or concurrent organ transplant Previous or concurrent malignancy Untreated proliferative diabetic retinopathy Unstable cardiovascular status, including positive stress echocardiography (if > age 35) Active infections, including x-ray evidence of pulmonary infection Peptic ulcer disease, gall stones, or portal hypertension Abnormal liver function tests Presence of panel reactive antibodies > 20% Creatinine clearance < 60 ml/min HbA1c > 12% Serological evidence of HIV, HbsAg, or HCV Anemia (hemoglobin < 12.0) Any condition or circumstance, including psychogenic factors, that preclude therapeutic compliance or otherwise make it unsafe to undergo an islet cell transplant. PSA > 4 in males

Sites / Locations

  • University of Miami Diabetes Research Institute

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 4, 2001
Last Updated
March 1, 2010
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00021801
Brief Title
Islet Cell Transplantation Alone and CD34+ Enriched Bone Marrow Cell Infusion in Patients With Diabetes Mellitus: Steroid-Free Regimen
Official Title
Pathways to Tolerance in Human Islet Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
March 2010
Overall Recruitment Status
Completed
Study Start Date
March 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2000 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

5. Study Description

Brief Summary
The goal of islet cell transplantation in Type 1 diabetics is to provide those affected with constant normal blood glucose levels, thereby reducing or eliminating altogether the need for injected insulin. This normalization may prevent or slow progression of diabetic complications, result in a healthier lifestyle, and lead to a better quality of life. Participants who meet the inclusion criteria will undergo an extensive screening process which typically includes a series of blood tests, EKG, chest x-rays, and a psychological evaluation, among others. Those who are eligible for and chose to participate in the trial will receive an islet cell transplant and bone marrow infusion from the same donor, together with following immunosuppressive medications: tacrolimus, sirolimus, daclizumab and infliximab. Because the bone marrow infusion may successfully prevent the transplanted islet cells from rejecting, some participants may be able to stop taking the immunosuppressive medications after a year. The islet cell transplant is done under local anesthesia in a special procedure radiology room. Several days after the islet cell transplant, the participant is admitted to the hospital as an outpatient in order to receive bone marrow via a simple intra-venous infusion procedure. All participants will need to be seen at the Diabetes Research Institute after the transplant for follow-up testing and post-islet cell transplant care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus
Keywords
Type I Diabetes Mellitus, Immunosuppression, Islet Cell Transplant, Percutaneous Transhepatic Portal

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Masking
None (Open Label)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Islet Cell Transplantation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Candidates must be between the ages of 18 and 50. Candidates must have had insulin-dependent diabetes mellitus (IDDM) for at least 5 years and been under physician care for at least 6 months prior to enrollment in trial. Eligible candidates will have poorly controlled IDDM and manifest signs and symptoms severe enough to be incapacitating. These symptoms can include episodes of hypoglycemic unawareness (failure to recognize blood glucose levels < 54 mg/dl) or episodes requiring the assistance of others. Candidates may have poor diabetes control despite intensive insulin therapy (HbA1c > 8.0%). Creatinine clearance should be > 60 ml/min) Body Mass Index should be less than 26 Women of child-bearing age must have a negative pregnancy test and agree to follow effective contraceptive measures for the duration of the trial. Exclusion Criteria: Previous or concurrent organ transplant Previous or concurrent malignancy Untreated proliferative diabetic retinopathy Unstable cardiovascular status, including positive stress echocardiography (if > age 35) Active infections, including x-ray evidence of pulmonary infection Peptic ulcer disease, gall stones, or portal hypertension Abnormal liver function tests Presence of panel reactive antibodies > 20% Creatinine clearance < 60 ml/min HbA1c > 12% Serological evidence of HIV, HbsAg, or HCV Anemia (hemoglobin < 12.0) Any condition or circumstance, including psychogenic factors, that preclude therapeutic compliance or otherwise make it unsafe to undergo an islet cell transplant. PSA > 4 in males
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodolfo Alejandro, MD
Organizational Affiliation
University of Miami Diabetes Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Miami Diabetes Research Institute
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
9392484
Citation
Alejandro R, Lehmann R, Ricordi C, Kenyon NS, Angelico MC, Burke G, Esquenazi V, Nery J, Betancourt AE, Kong SS, Miller J, Mintz DH. Long-term function (6 years) of islet allografts in type 1 diabetes. Diabetes. 1997 Dec;46(12):1983-9. doi: 10.2337/diab.46.12.1983.
Results Reference
background
PubMed Identifier
19005394
Citation
Tharavanij T, Betancourt A, Messinger S, Cure P, Leitao CB, Baidal DA, Froud T, Ricordi C, Alejandro R. Improved long-term health-related quality of life after islet transplantation. Transplantation. 2008 Nov 15;86(9):1161-7. doi: 10.1097/TP.0b013e31818a7f45.
Results Reference
derived

Learn more about this trial

Islet Cell Transplantation Alone and CD34+ Enriched Bone Marrow Cell Infusion in Patients With Diabetes Mellitus: Steroid-Free Regimen

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