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Pilot Study- Treat to Target Vitamin D in End Stage Renal Disease

Not Applicable
Withdrawn
Conditions
Chronic Kidney Diseases
Registration Number
NCT04167111
Lead Sponsor
University of Nebraska
Brief Summary

Feasibility of dose adjustment to reach a 6 month 25-hydroxy vitamin D level of 35-50 ng/ml in end stage renal disease patients

Detailed Description

Pilot study to test the feasibility of adjusting doses based on a prespecified algorithm to reach a 6 month 25(OH)D level of 35-50 ng/ml in end stage renal disease patients.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • likely be able to complete the study, >3 months on hemodialysis, receiving standard of care through their nephrologist.
Exclusion Criteria
  • on peritoneal dialysis, allergy to vitamin D, liver disease, intestinal disorders that interfere with vitamin D absorption, taking vitamin D >800 IU per day, 25(OH)D level >30 ng/ml, glucocorticoids, anticonvulsants or drug therapies for osteoporosis, pregnancy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Primary Outcome Measures
NameTimeMethod
25(OH)D level6 months

25(OH)D level

Secondary Outcome Measures
NameTimeMethod

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