Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:39 AM
Ignite Modification Date:
2025-12-25 @ 1:39 AM
NCT ID:
NCT00285194
Eligibility Criteria:
Inclusion Criteria:
1. Primary islet allotransplant
2. Type 1 diabetes mellitus, complicated by at least one of the following situations that persist despite intensive efforts in close cooperation with their diabetes care team:
1. Metabolic lability/instability;
2. Reduced awareness of hypoglycemia;
3. Persistently poor glucose control (as defined by HgbA1c\>10% at the end of six months of intensive management efforts with the diabetes care team);
4. Progressive secondary complications.
3. Age 18 and older
4. Able to give written informed consent
Exclusion Criteria:
1. Age less than 18 years
2. Body weight greater than75 kg.
3. BMI greater than 26 kg/m2 for male and females
4. Waist-to-hip ratio 0.80 (female) and 0.95 (male)
5. First degree relative with type 2 diabetes
6. Insulin requirement of greater than 0.7 IU/kg/day
7. HbA1C greater than 12%
8. Positive C-peptide response to intravenous arginine stimulation
9. Untreated proliferative retinopathy
10. Macroalbuminuria (urinary albumin excretion greater than 300 mg/24hrs)
11. Creatinine clearance greater than 85 ml/min/1.73 m2 in females, greater than 95 ml/min/1.73 m2 in males
12. Serum creatinine greater than 1.2 mg/dl
13. Previous pancreas or islet transplant
14. Previous OKT3 antibody therapy
15. Presence of history of panel-reactive anti-HLA antibodies greater than 10%
16. Abnormal T4 and TSH despite thyroid replacement therapy
17. Positive pregnancy test, or presently breast-feeding
18. Active infection
19. Negative screen for Epstein-Barr Virus (EBV) by an EBNA method
20. Invasive aspergillus infection within year prior to study entry
21. Any history of malignancy
22. Active alcohol or substance abuse
23. History of non-adherence to prescribed regimens
24. Psychiatric disorder making the subject not a suitable candidate for transplantation
25. Karnofsky performance score greater than 70
26. Baseline Hgb greater than 11.7 g/dl; lymphopenia (greater than 1,000/L), or leukopenia (greater than 4,000 total leukocytes/L), or an absolute CD4+ count \<500/L
27. Thrombocytopenia greater than 150 x 109/L
28. Use of warfarin or other anticoagulant therapy (except aspirin) or patient with PT-INR greater than 1.5
29. Severe co-existing cardiac disease
30. Baseline liver function tests outside of normal range
31. Presence of gallstones on baseline ultrasound exam
32. Active peptic ulcer disease
33. Severe unremitting diarrhea or other gastrointestinal disorders potentially interfering with the ability to absorb oral medications
34. Celiac disease
35. Hyperlipidemia (fasting LDL cholesterol greater than 130 mg/dl, treated or untreated; and/or fasting triglycerides greater than 200 mg/dl)
36. Addison's disease.
37. Under treatment for a medical condition requiring chronic use of systemic steroids
38. Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT00285194
Study Brief:
Protocol Section:
NCT00285194