This open-label study will determine if chlorthalidone is safe and effective for the use of reducing urinary calcium excretion over 4 weeks in subjects with type 1 diabetes
Type 1 diabetes (T1D) is associated with increased urinary calcium loss, which may contribute to the low bone mineral density and increased fracture risk observed in patients with this condition. Chlorthalidone is a thiazide-like diuretic that is commonly used to reduce urinary calcium excretion in other conditions such as idiopathic hypercalciuria. Its safety and efficacy has not been specifically tested in an adolescent type 1 diabetes population. T1D subjects with hypercalciuria and who meet inclusion/exclusion criteria will be given chlorthalidone daily. Blood and urine tests, blood pressure, and glycemic control will be assessed at weekly study visits for 4 weeks.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
1
Chlorthalidone 12.5-5 mg by mouth daily for 4 weeks
University of Rochester
Rochester, New York, United States
Urinary Calcium Excretion
Change in 24 hour urine calcium excretion
Time frame: Assessed at baseline and at 4 weeks
Hypokalemia
Serum potassium decreased to \<3.5 milliequivalent/L
Time frame: Assessed weekly for up to 4 weeks or until hypokalemia develops
Hypercalcemia
Serum calcium increased to \>10.5 mg/dL
Time frame: Assessed weekly for up to 4 weeks or until hypercalcemia develops
Hyperglycemia
Change in serum fructosamine
Time frame: Assessed at baseline and at 4 weeks
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