Eligibility Module

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: 2025-12-24 @ 4:31 PM
Ignite Modification Date: 2025-12-24 @ 4:31 PM
NCT ID: NCT00175266
Eligibility Criteria: Inclusion Criteria: * must have Type 1 diabetes mellitus for more than 5 years * diabetes must be complicated by at least one of the following situations that persist despite intensive insulin management efforts. The complicating situations are (1) Reduced awareness of hypoglycemia, as defined by the absence of adequate autonomic symptoms at plasma glucose levels of \< 3.0 mmol/L; (2) Metabolic lability/instability, characterized by MAGE ≥ 11.0 mmol/L and wide swings in blood glucose despite optimal diabetes therapy; and (3) Despite efforts at optimal glucose control, progressive secondary complications of diabetes, including retinopathy, neuropathy, or nephropathy Exclusion Criteria: * Severe co-existing cardiac disease * Active alcohol or substance abuse * Psychiatric disorder making the subject not a suitable candidate for transplantation * Active infection including hepatitis C, hepatitis B, HIV, or TB * Any history of or current malignancies except squamous or basal skin cancer * BMI \> 28 kg/m2 or body weight \> 85 kg at screening visit * Positive fasting C-peptide response on assessment (2 positive results) * Creatinine clearance \< 80 mL/min/1.73 m2 * Serum creatinine \> 150 µmol/L * Macroalbuminuria (urinary albumin excretion rate \> 300 mg/24h) * Baseline Hb \< 105g/L in women, or \< 130 g/L in men * Baseline LFT's outside of normal range * Untreated proliferative retinopathy * Positive pregnancy test, intent for future pregnancy or male subjects' intent to procreate, failure to follow effective contraceptive measures, or presently breast feeding * Previous transplant, or evidence of sensitization on PRA * Insulin requirement \> 1.0 IU/kg/day * HbA1C \> 0.12 * Hyperlipidemia (fasting LDL cholesterol \> 3.4 mmol/L, treated or untreated; and/or fasting triglycerides \> 2.3 mmol/L) * Under treatment for a medical condition requiring chronic use of steroids * Use of coumadin or other anticoagulant therapy (except aspirin) or subject with PT INR \> 1.5 * Untreated Addison's disease * Untreated Celiac disease * Untreated thyroid disease
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 65 Years
Study: NCT00175266
Study Brief:
Protocol Section: NCT00175266