Screening of Subjects With Type I Diabetes to Determine Eligibility for Islet Transplantation

NCT ID: NCT02004964

Last Updated: 2018-12-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-04-30

Study Completion Date

2018-11-06

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Protocol to screen potential subjects for islet transplantation

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Subjects with Type 1 diabetes and history of severe hypoglycemia will undergo screening similar to the screening done for islet transplantation including: history; physical; chest X rays; upper GI series if history of ulcer; abdominal and pelvic ultrasound with careful attention to liver parenchyma and gallbladder; EKG; stress echocardiography if older than 35, psychological evaluation; autonomic and sensorimotor evaluation. They will also have a tuberculosis skin test (PPD), and pre-transplant laboratory tests, including: serology (for hepatitis B and C, HTLV I and II, Herpesvirus 1 and 2, CMV, EBV, Parvovirus B19, RPR and HIV); first morning urine (albumin, protein and creatinine), GFR; urinalysis and urine culture; CBC, chemistry, PT, PTT, INR, C-peptide (basal and stimulated), HbA1c, , lipid profile, LFTs, thyroid profile, blood typing, PRA, MHC determination, auto-antibodies (GAD65, IA2 and insulin), and if male, prostate specific antigen (PSA). Severity of glucose lability and hypoglycemia unawareness is assessed with Clarke score, Lability index, Mage and hypoglycemia score.

I

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Type 1 Diabetes Mellitus

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Patients between 18 and 65 years of age
2. Patients with type 1 diabetes mellitus for more than 5 years duration
3. Body Mass Index (BMI)
4. Fulfill one or more of the following:

1\. Manifest signs and symptoms that are severe enough to be incapacitating. Incapacitating signs and symptoms include hypoglycemic episodes requiring assistance by others and hypoglycemia unawareness, (the inability to recognize low blood glucoses; glucoses \<54 mg/dl); and/or 2. Patients with poor diabetes control (HbA1c \> 8.0% but \< 12%), despite intensive insulin therapy, as defined by: self monitoring of blood glucose ≥ 4 times/day, and multiple insulin injections (≥ 3/day) or insulin pump, and close monitoring of blood glucose control by an Endocrinologist.; and/or 3. Progressive diabetic complications.

Exclusion Criteria

1. Age \<18 or \>65 years;
2. Duration of diabetes \<5 years;
3. Do not have a physician that is monitoring diabetes for \> 6 months;
4. Body Mass Index \>30
5. Weight \>80 kg;
6. Insulin requirement \>1.0 u/kg/d;
7. HbA1C \>12%;
8. Stimulated or basal C-peptide \>0.3 ng/ml;
9. Iohexol GFR\<80
10. Macroalbuminuria (\>300 mg/24 hours);
11. Anemia consistently lower than the normal range.
12. Hyperlipidemia (fasting LDL cholesterol\>130mg/dl and/or fasting triglycerides \>200mg/dl);
13. Abnormal liver function tests (consistently \>1.5 x normal range);
14. Serological evidence of HIV, HBsAg and/or HBcAb, HBsAb without history of vaccination, HTLV-1 or HCV;
15. Negative serology for Epstein Barr virus (EBV) or evidence of acute or chronic infection (IgM≥IgG);
16. Lack of updated immunizations per current CDC guidelines (including Lack of immunization against hepatitis B, pneumococcus and influenza - during season);
17. Presence of panel reactive antibodies by flow cytometry
18. Prostate specific antigen (PSA) \>4 ng/ml unless malignancy ruled out;
19. Positive tuberculin test (unless proof of adequate treatment can be provided);
20. X-ray evidence of pulmonary infection or other significant pathology;
21. Gall stones and/or portal hypertension and/or hemangioma on liver ultrasound;
22. Abnormal abdominal or pelvic ultrasound (evidence of masses that are considered suspicious for malignancy or adenopathy);
23. Active peptic ulcer disease;
24. Active infections;
25. Unstable cardiovascular status (including positive stress echocardiography if \>age 35)/MI in the past 6 months/LVEF\<30%)
26. Untreated or unstable proliferative diabetic retinopathy;
27. Previous/concurrent organ transplantation (except failed islet cell / pancreas transplantation);
28. Malignancy or previous malignancy;
29. Any medical condition requiring chronic use of steroids;
30. Active alcohol or substance abuse; smoking in the last 6 months;
31. Sexually active females who are not: a) post-menopausal, b) surgically sterile, or c) not using an acceptable method of contraception (oral contraceptives, Norplant, Depo-Provera, and barrier devices with spermicide are acceptable; condoms used alone are not acceptable);
32. Positive pregnancy test or intent for future pregnancy, or male subject's intent to procreate;
33. Any condition or any circumstances that makes it unsafe to undergo an islet cell transplant;
34. Psychogenically unable to comply;
35. Failed psychological evaluation.
36. Persistent leukopenia (white blood cell count \<3,000/uL on more than 3 occasions)
37. Acute or chronic pancreatitis.
38. Severe or unremitting diarrhea, vomiting or othe gastrointestinal disorder potentially interfering with the ability to absorb oral medications.
39. Lymphopenia - \< 1,000/uL 40 Neutropenia - \<1,500/uL

41\. Thrombocytopenia - \<100,000/uL
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Rodolfo Alejandro

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Rodolfo Alejandro

Professor of Medicine

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Rodolfo Alejandro, MD

Role: PRINCIPAL_INVESTIGATOR

University of Miami

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Diabetes Research Institute

Miami, Florida, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

20053135

Identifier Type: -

Identifier Source: org_study_id