Status:
COMPLETED
Vitamin D and Arteriovenous Fistulae
Lead Sponsor:
Emory University
Conditions:
End-stage Renal Disease
Eligibility:
All Genders
18-85 years
Phase:
NA
Brief Summary
Patients requiring hemodialysis following kidney failure need a form of dialysis vascular access in order to undergo the dialysis procedure. Dialysis vascular access dysfunction is an enormous clinica...
Detailed Description
Hemodialysis vascular access dysfunction is a major source of morbidity and cost among ESRD patients, accounting for up to 25% of all hospital stays, and 50% of all costs within the first year of init...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Patients with patients with end-stage renal disease (ESRD) who are suitable candidates for AVF creation (as assessed by pre-operative vein mapping) and plan to undergo AVF creation are eligible to participate
- Study subjects must agree to participate in the study and provide written informed consent
- Age: Study subjects must be \> 18 years old
- Sites: Emory University affiliated hospitals (including Emory University Hospital, Emory Midtown Hospital, Grady Memorial Hospital) and Emory University affiliated outpatient dialysis units
- Informed consent requirements: All study subjects must agree to participate in the study and provide written informed consent.
- Exclusion Criteria
- Age \< 18 years
- Patients with a corrected serum calcium \> 10.5 mg/dL within 4 weeks of study screening
- Current intake of \> 2000 IU per day of Vitamin D3
- Subjects unable to provide informed consent or who plan to relocate outside of Atlanta during the study duration
Exclusion
Key Trial Info
Start Date :
January 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2011
Estimated Enrollment :
52 Patients enrolled
Trial Details
Trial ID
NCT00912782
Start Date
January 1 2009
End Date
June 1 2011
Last Update
July 2 2014
Active Locations (1)
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1
Emory University
Atlanta, Georgia, United States, 30322