search
Back to results

Islet Cell Transplantation Alone in Patients With Type I Diabetes Mellitus: Steroid-free Immunosuppression

Primary Purpose

Diabetes Mellitus, Type 1

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 Diabetes Mellitus, Type 1 focused on measuring Type I Diabetes Mellitus, Immunosuppression, Islet Cell Transplantation, PercutaneousTranshepaticPortalVein Catheterization

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Candidates must be between the ages of 18 and 65 Candidates must have had 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 insulin-dependent diabetes mellitus (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
July 7, 2010
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
search

1. Study Identification

Unique Protocol Identification Number
NCT00021788
Brief Title
Islet Cell Transplantation Alone in Patients With Type I Diabetes Mellitus: Steroid-free Immunosuppression
Official Title
Immunomodulation for Islet Transplantation in Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
July 2010
Overall Recruitment Status
Completed
Study Start Date
July 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2001 (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 patients with Type 1 Diabetes Mellitus is to provide constant normal blood glucose levels. This may eliminate the need for insulin altogether or provide a significant reduction in the amount of insulin necessary to maintain constant normal blood glucose levels. This normalization may prevent or slow progression of diabetic complications. Furthermore, the participant may enjoy a healthier lifestyle and a better quality of life. If you meet the initial inclusion criteria for the trial, you must be able to give informed consent personally. Then you will need to participate in an extensive screening process that involves many standard tests and collection of laboratory samples to make sure that the transplant is suitable and safe for you.
Detailed Description
The trial may/will utilize the following immunosuppressive medications: tacrolimus (life-long), sirolimus (life-long), daclizumab and infliximab You will be maintained on the lowest doses possible with all the medications. GROUP (1A): The first four participants will be assigned to Group A. These participants will receive an islet cell transplant alone from two donors. They will receive the following immunosuppressive medications: tacrolimus (lifelong), sirolimus (lifelong), and daclizumab. They will not receive the immunosuppressive medication infliximab. GROUP (1B): The second four participants will be assigned to group B. These participants will receive an islet cell transplant alone from one donor. They will receive the following immunosuppressive medications: tacrolimus (lifelong), sirolimus (lifelong), daclizumab and infliximab. Patients in this group who are not able to stop injecting insulin by three months after the transplant may be eligible to receive a second islet cell transplant. Further participants will alternate group assignments in the same above-mentioned manner. The participants in both groups will receive the following immunosuppressive medications for life, tacrolimus and sirolimus. All participants will be required to live no more than two hours from the transplantation center. When the islets become available, you will be notified to come immediately to the hospital for your transplant. At that time numerous tests and laboratory samples will be performed to make sure you are ready and healthy for your transplant. You will have your islet cell transplant done in a special radiology procedure room in a hospital. You will have local anesthetic in the area of your liver on your right side along with sedatives that will minimize any discomfort the procedure might cause. A very small (thin) needle will be inserted through your liver into your portal vein where the islet cells are then injected. All participants will need to be followed at the Diabetes Research Institute after transplant for laboratory sampling, testing and for general islet cell transplant care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1
Keywords
Type I Diabetes Mellitus, Immunosuppression, Islet Cell Transplantation, PercutaneousTranshepaticPortalVein Catheterization

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
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Candidates must be between the ages of 18 and 65 Candidates must have had 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 insulin-dependent diabetes mellitus (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
Study Director
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
10665560
Citation
McAlister VC, Gao Z, Peltekian K, Domingues J, Mahalati K, MacDonald AS. Sirolimus-tacrolimus combination immunosuppression. Lancet. 2000 Jan 29;355(9201):376-7. doi: 10.1016/S0140-6736(99)03882-9.
Results Reference
background

Learn more about this trial

Islet Cell Transplantation Alone in Patients With Type I Diabetes Mellitus: Steroid-free Immunosuppression

We'll reach out to this number within 24 hrs