Two Vitamin D Dosing Strategies in Children With Chronic Kidney Disease
Primary Purpose
Chronic Kidney Disease
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
1000 IU of Vitamin D3
4000 IU of Vitamin D3
Sponsored by

About this trial
This is an interventional treatment trial for Chronic Kidney Disease
Eligibility Criteria
Inclusion Criteria:
- Patient's parent/legal guardian must be willing and able to give written informed consent and the patient must be willing to give written informed assent if applicable
- Estimated glomerular filtration rate < 60 mL/min/1.73 m2 body surface area or recipient of a kidney transplant
- 9-21 years old
- Able to swallow pills
Exclusion Criteria:
- Liver failure
- Malabsorption
- Current calcium level >10.5 mg/dL
- History of hypercalcemia (Ca >11 mg/dL) during the preceding 6 months
- Current treatment with an antiepileptic drug or other medications that may affect vitamin D metabolism (e.g., phenobarbital, phenytoin, rifampicin)
- History of hypervitaminosis D
- Completion of a course of high dose vitamin D within the preceding 2 months
Sites / Locations
- Childen's Healthcare of Atlanta
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
1000 IU of Vitamin D Daily
4000 IU of Vitamin D Daily
Arm Description
Participants randomized to take a 1000 IU capsule of Vitamin D every day for 6 months.
Participants randomized to take a 4000 IU capsule of Vitamin D capsule every day for 6 months.
Outcomes
Primary Outcome Measures
Percentage of Participants with Adequate Vitamin D Level
Vitamin D sufficiency will be assessed as the percentage of participants with a vitamin D level >30 ng/ml.
Secondary Outcome Measures
Full Information
NCT ID
NCT01909115
First Posted
July 24, 2013
Last Updated
May 17, 2020
Sponsor
Emory University
Collaborators
Children's Healthcare of Atlanta
1. Study Identification
Unique Protocol Identification Number
NCT01909115
Brief Title
Two Vitamin D Dosing Strategies in Children With Chronic Kidney Disease
Official Title
Randomized Trial of Two Maintenance Doses of Vitamin D and Trace Element Status in Children With Chronic Kidney Disease
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
September 2013 (Actual)
Primary Completion Date
September 26, 2014 (Actual)
Study Completion Date
September 26, 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Children's Healthcare of Atlanta
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Vitamin D deficiency is common in the general population and more common in children with chronic kidney disease. Vitamin D is very important for bone health, especially in children with chronic kidney disease. To date, several studies using different doses of vitamin D have been tried to correct vitamin D deficiency, but none has been completely successful. The investigators are comparing two different doses of vitamin D to determine which one is more effective at correcting and maintaining normal blood levels of vitamin D. The investigators hypothesize that a higher percentage of children receiving a higher dose of vitamin D will be vitamin D replete at the end of 6 months.
This study will enroll 80 children 9 to 18 years old who have chronic kidney disease (CKD) and can take pills. They will be enrolled from Chronic Renal Insufficiency Clinic, the Hemodialysis Unit, Peritoneal Dialysis Clinic and Transplant Clinic at Children's Healthcare of Atlanta.
Detailed Description
Vitamin D has a critical role in bone metabolism. In addition, there is increasing evidence that vitamin D has an important role in many other areas, including cardiovascular health, immune function, and prevention of autoimmune diseases and certain malignancies. In patients with CKD, there are a variety of abnormalities in mineral metabolism that lead to bone disease.
After the investigators obtain informed consent and assent, children will be randomly assigned to either low dose (1000 units daily) or high dose (4000 units daily) vitamin D pills (50% in each group). Participants will take vitamin D capsules every day for for 6 months. Vitamin D levels will be obtained at baseline, 3 months and 6 months. The study visits will be at the same time as routine clinic visits when the children are having blood drawn for routine care. At the end of the study, the investigators will compare the percentage of patients who have normal vitamin D levels at 6 months in the two groups. The investigators will also describe the percentage of patients who have elevated or low levels of trace elements.
The two doses of vitamin D in this study are within the dosing range recommended by the Institute of Medicine, and thus the investigators do not anticipate any adverse effects. Vitamin D toxicity could theoretically occur, and an elevated vitamin D level at 3 months would be an indication to withdraw a patient from the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
98 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1000 IU of Vitamin D Daily
Arm Type
Active Comparator
Arm Description
Participants randomized to take a 1000 IU capsule of Vitamin D every day for 6 months.
Arm Title
4000 IU of Vitamin D Daily
Arm Type
Experimental
Arm Description
Participants randomized to take a 4000 IU capsule of Vitamin D capsule every day for 6 months.
Intervention Type
Drug
Intervention Name(s)
1000 IU of Vitamin D3
Intervention Description
1000 IU of Vitamin D will be administered in capsule form, once daily.
Intervention Type
Drug
Intervention Name(s)
4000 IU of Vitamin D3
Intervention Description
4000 IU of Vitamin D will be administered in capsule form, once daily.
Primary Outcome Measure Information:
Title
Percentage of Participants with Adequate Vitamin D Level
Description
Vitamin D sufficiency will be assessed as the percentage of participants with a vitamin D level >30 ng/ml.
Time Frame
Month 6
10. Eligibility
Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient's parent/legal guardian must be willing and able to give written informed consent and the patient must be willing to give written informed assent if applicable
Estimated glomerular filtration rate < 60 mL/min/1.73 m2 body surface area or recipient of a kidney transplant
9-21 years old
Able to swallow pills
Exclusion Criteria:
Liver failure
Malabsorption
Current calcium level >10.5 mg/dL
History of hypercalcemia (Ca >11 mg/dL) during the preceding 6 months
Current treatment with an antiepileptic drug or other medications that may affect vitamin D metabolism (e.g., phenobarbital, phenytoin, rifampicin)
History of hypervitaminosis D
Completion of a course of high dose vitamin D within the preceding 2 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Larry Greenbaum, MD, PhD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Childen's Healthcare of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
34392411
Citation
Nadeem S, Tangpricha V, Ziegler TR, Rhodes JE, Leong T, Xiang Y, Greenbaum LA. Randomized trial of two maintenance doses of vitamin D in children with chronic kidney disease. Pediatr Nephrol. 2022 Feb;37(2):415-422. doi: 10.1007/s00467-021-05228-z. Epub 2021 Aug 15.
Results Reference
derived
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Two Vitamin D Dosing Strategies in Children With Chronic Kidney Disease
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