Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Descrizione dettagliata
- To reverse hyperglycemia and insulin dependency by islet cell transplantation, in patients with Type 1 Diabetes Mellitus who have a stable kidney allograft;
- To eliminate the incidence of hypoglycemic coma and unawareness by islet cell transplantation;
- To assess long-term function of successful islet cell transplants;
- To determine whether the natural history of the microvascular, macrovascular and neuropathic complications of Diabetes Mellitus are altered following successful transplantation of islet cells.
- To assess the effect of exenatide to improve islet graft function and survival in subjects that demonstrate partial graft loss and have returned to using exogenous insulin.
- To assess the ability of exenatide to improve islet survival at time of islet transplantation
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
-
-
Florida
-
Miami, Florida, Stati Uniti, 33136
- Diabetes Research Institute
-
-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Patients between 18 and 60 years of age.
- Patients with type 1 diabetes mellitus.
- Patients with a renal transplant that is more than 6 months old.
- Patients with stable renal graft function for the preceding 6 months, i.e. no episodes of rejection and changes in serum creatinine no more than 0.5 mg/dl from baseline.
- Patients who are taking tacrolimus, sirolimus +/- steroids for maintenance immunosuppression for at least 6 months and are tolerating levels satisfactory for islet transplantation without severe complications.
- Patients with a body mass index (BMI) of less than or equal to 26.
Exclusion Criteria:
- Stimulated or basal C-peptide > 0.3 ng/ml.
- Patients with unstable renal function - serum creatinine greater than 0.5 mg/dl above baseline.
- Patients with proteinuria (albuminuria > 300 mg in 24 hours +/- protein) of new onset since kidney transplantation. If proteinuria or albuminuria is thought to originate from the native kidney(s) this will not be an exclusion criterion.
- Patients with corrected creatinine clearance of less than 40.
- Patients weighing more than 80 kg.
- Patients with a body mass index (BMI) of greater than 26.
- Insulin requirement > 1.0 U/kg/d.
- Anemia (hemoglobin: males < 11.0 g/dl; females < 10.0 g/dl).
- Abnormal liver function tests (consistently > 1.5 x normal range).
- Unstable diabetic retinopathy.
- Evidence of acute or chronic active Epstein-Barr virus (EBV) infection (IgM ≥ IgG). Patients will be eligible if serological testing becomes consistent with previous exposure (i.e. IgG > IgM).
- Patients with history of malignancy or current malignancy other than non-melanomatous skin cancer, or finding of any lesions or symptoms during screening that are suspicious for malignancy, until properly investigated and ruled out.
- Patients with elevation of prostate-specific antigen > 4 unless malignancy has been excluded.
- Patients with unstable cardiovascular status.
- Patients with active infections until adequately treated, unless treatment is not judged as necessary by the investigators (including, but not limited to, mild skin and nail fungal infections).
- Patients with serological evidence of infection with HIV, human t cell lymphotropic virus 1 (HTLV 1), HTLV 2, or hepatitis B (patients with serology consistent with previous vaccination and a history of vaccination are acceptable).
- Patients with history and/or serological evidence of hepatitis C (those patients with hepatitis C, already transplanted in this protocol will continue in this trial).
- Positive tuberculin test (unless proof of adequate treatment for latent tuberculosis can be provided).
- Patients with active peptic ulcer disease, gallstones, hepatic hemangioma, or portal hypertension.
- Patients who are pregnant or breastfeeding, or who intend to procreate.
Patients who are sexually active females who are not:
- post-menopausal,
- surgically sterile, or
- using an acceptable method of contraception (oral contraceptives, Norplant, Depo-Provera, and barrier devices combined with spermicidal gel are acceptable; condoms used alone are not acceptable).
- Active alcohol or substance abuse; smoking in the last 6 months.
- Patients with evidence of sensitization, i.e. panel reactive antibody (PRA) testing greater than 20%.
- Lack of updated immunizations per current Centers for Disease Control (CDC) guidelines, as well as immunization against hepatitis B, pneumococcus, and influenza (during season), unless medically contraindicated.
- Patients with psychogenic factors, which are judged at psychological evaluation, which make it unsafe to undergo islet transplantation, or which preclude therapeutic compliance.
- Patients with any condition or any circumstance that would make it unsafe to undergo an islet transplant.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
|
Sperimentale: Islet Transplantation
Islet Transplantation in subjects with a previous kidney transplant.
|
Islet Transplantation in subjects with a previous kidney transplant.
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Insulin Independence.
Lasso di tempo: 1 year
|
Number of Participants who Achieved Insulin Independence at 1 Year
|
1 year
|
Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Stimulated C-peptide Greater Than 0.5 ng/ml
Lasso di tempo: 1 year
|
Partial graft function, as evidenced by basal C-peptide greater than 0.5 ng/ml
|
1 year
|
|
Reduction of Insulin Requirements
Lasso di tempo: 1year
|
Reduction in insulin requirements in those patients who do not achieve insulin independence
|
1year
|
|
Reduction in Severe Hypoglycemia, Improvement in Hypoglycemia Awareness
Lasso di tempo: 1 years
|
Elimination or reduction in the incidence of hypoglycemic coma or unawareness
|
1 years
|
Collaboratori e investigatori
Sponsor
Sponsor
Collaboratori
Collaboratori
Investigatori
Investigatori
- Investigatore principale: Rodolfo Alejandro, M.D., University of Miami
Pubblicazioni e link utili
Pubblicazioni generali
- 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.
- Faradji RN, Froud T, Messinger S, Monroy K, Pileggi A, Mineo D, Tharavanij T, Mendez AJ, Ricordi C, Alejandro R. Long-term metabolic and hormonal effects of exenatide on islet transplant recipients with allograft dysfunction. Cell Transplant. 2009;18(10):1247-59. doi: 10.3727/096368909X474456.
- Cure P, Pileggi A, Froud T, Messinger S, Faradji RN, Baidal DA, Cardani R, Curry A, Poggioli R, Pugliese A, Betancourt A, Esquenazi V, Ciancio G, Selvaggi G, Burke GW 3rd, Ricordi C, Alejandro R. Improved metabolic control and quality of life in seven patients with type 1 diabetes following islet after kidney transplantation. Transplantation. 2008 Mar 27;85(6):801-12. doi: 10.1097/TP.0b013e318166a27b.
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Effettivo)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 2000/0329
- 5R01DK055347 (Sovvenzione/contratto NIH degli Stati Uniti)
- 5R01DK025802 (Sovvenzione/contratto NIH degli Stati Uniti)
Piano per i dati dei singoli partecipanti (IPD)
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