Type I Diabetes Clinical Trial
Official title:
Anti-IL-1 Treatment in Children Diabetic Keto-Acidosis (DKA) at Diagnosis of Type 1 Diabetes.
Verified date | April 2019 |
Source | University of Colorado, Denver |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized, double-blind, placebo-controlled phase 2 study. Specific aim is to evaluate feasibility and safety of anti-IL-1 (interleukin 1) treatment in the course of standard therapy for diabetic ketoacidosis in children and its effect on intracranial pressure.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | April 22, 2016 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 8 Years to 18 Years |
Eligibility |
Inclusion Criteria: - Age 8-18 years at diagnosis of type 1 diabetes - Diabetic ketoacidosis with: - plasma glucose concentration >300 mg/dl, - venous pH <7.30 or - serum bicarbonate concentration <15 mmol/L, and - ketones in urine or serum - Hematology: - WBC >3000 x 109/L; - platelets >100,000 x 109/L; - hemoglobin >10.0 g/dL - Negative blood pregnancy test in females. Exclusion Criteria: - Children with underlying disorders, including: - active autoimmune or immune deficiency disorder other than type 1 diabetes, - malignancy, - organ transplant, - any condition requiring chronic corticosteroid use - Previous immunotherapy to prevent type 1 diabetes - Current or prior infection with HIV, hepatitis B or hepatitis C assessed by history - Patients who present with DKA concomitant with alcohol or drug use, - Head trauma, - Meningitis or other conditions which might affect neurological function - Renal failure - Any condition, medical or otherwise that would, in the opinion of the investigator, prevent complete participation in the study, or that would pose a significant hazard to the subject's participation - Patients with a history of known hypersensitivity to: - E coli-derived proteins, - anakinra, or - any components of the investigational drug product |
Country | Name | City | State |
---|---|---|---|
United States | Childrens Hospital Colorado | Aurora | Colorado |
United States | University of Colorado, Anschutz Medical Campus | Aurora | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Denver | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
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* Note: There are 42 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Frequency of Adverse Events | Type and number of Adverse Events related to anti-IL-1 treatment (anakinra) during the initial 24 hour period of DKA treatment. | 24 hours |
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