Impact of Vitamin D Therapies on Chronic Kidney Disease
Primary Purpose
Chronic Kidney Disease (CKD), End-stage Renal Disease (ESRD)
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cholecalciferol - CKD
Calcitriol - CKD
Cholecalciferol - non-CKD
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Kidney Disease (CKD)
Eligibility Criteria
Inclusion Criteria:
- Chronic kidney disease w/GFR<35ml/min
- Nutritional vitamin D deficiency, defined as 25(OH)D < 25ng/ml
- Secondary hyperparathyroidism, PTH>75pg/mL
Exclusion Criteria:
- Active infection
- Recent hospitalization for acute illness (within last month)
- Refusal to study participation
- History of chronic inflammatory disease process (i.e. inflammatory bowel, rheumatoid arthritis, SLE, etc.)
- Allergy to cholecalciferol or calcitriol
- History of parathyroidectomy
- Functional renal transplant within 5 years
- Current treatment with immunosuppressant medications
- Noncompliance with prescribed medications
Sites / Locations
- University Of Kansas Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
Group 1: Cholecalciferol - CKD
Group 2: Calcitriol - CKD
Group 3: Cholecalciferol - non-CKD
Arm Description
Patients in this group have low vitamin D levels and Chronic Kidney Disease (CKD). They will be administered cholecalciferol 50,000 IU twice weekly for 8 weeks.
Patients in this group have low vitamin D levels and Chronic Kidney Disease (CKD). They will be administered calcitriol 0.25mcg daily for 8 weeks.
Patients in this arm have low vitamin D levels and normal kidney function. They will be administered cholecalciferol 50,000 IU twice weekly for 8 weeks.
Outcomes
Primary Outcome Measures
Monocyte Protein Expression
Flow cytometry analysis of monocyte CD14, ACE, VDR, and Mac-1 expression
Change in 24,25(OH)2D Levels in CKD vs. Non-CKD Subjects Receiving Cholecalciferol
Secondary Outcome Measures
Full Information
NCT ID
NCT01222234
First Posted
October 13, 2010
Last Updated
April 11, 2016
Sponsor
University of Kansas Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01222234
Brief Title
Impact of Vitamin D Therapies on Chronic Kidney Disease
Official Title
Impact of Vitamin D Therapies on Monocyte Function in Chronic Kidney Disease
Study Type
Interventional
2. Study Status
Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Kansas Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This investigation will consist of a prospective study utilizing two separate populations of patients with 25(OH)D deficiency, one population with chronic kidney disease (CKD) and one with normal renal function.
Detailed Description
Vitamin D helps form and strengthens bones by allowing the body to absorb calcium. Vitamin D helps the immune system fight infection as well as helps keep muscles strong. Without enough vitamin D, bones can become weak, thin and brittle.
Vitamin D is useful in people with all different types of health issues. CKD is the slow loss of kidney function over time. The main function of the kidneys is to remove wastes and excess water from the body. This loss of function usually takes months or years to occur Patients with CKD often have low levels of vitamin D in their blood.
This study will have two groups of patients with CKD and one group of patients that have normal kidney function, but all groups will have low levels of vitamin D. The two groups with CKD (group 1 and group 2) will receive either cholecalciferol or calcitriol. The purpose of having a control group (group 3) without CKD will be to evaluate if any changes that are witnessed in response to vitamin D therapy are specific to patients with kidney disease or apply to all patients with vitamin D deficiency who receive vitamin D supplements.
There are two different drugs in this study. One is called Calcitriol and is approved by the Food and Drug Administration (FDA) as a vitamin D supplement. The other drug is called cholecalciferol and it is approved by the FDA. Unlike calcitriol, cholecalciferol is a nutritional form of vitamin D that can often be found in various types of foods and its chemical structure must be changed by the body to become the active form of vitamin D. It is believed that cholecalciferol may have different effects in the body compared to calcitriol. It is possible that CKD patients would benefit from receiving both of these drugs, but this is currently unclear. While on this study you will receive either one of these study drugs, depending on which group you are assigned to.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease (CKD), End-stage Renal Disease (ESRD)
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group 1: Cholecalciferol - CKD
Arm Type
Experimental
Arm Description
Patients in this group have low vitamin D levels and Chronic Kidney Disease (CKD). They will be administered cholecalciferol 50,000 IU twice weekly for 8 weeks.
Arm Title
Group 2: Calcitriol - CKD
Arm Type
Experimental
Arm Description
Patients in this group have low vitamin D levels and Chronic Kidney Disease (CKD). They will be administered calcitriol 0.25mcg daily for 8 weeks.
Arm Title
Group 3: Cholecalciferol - non-CKD
Arm Type
Experimental
Arm Description
Patients in this arm have low vitamin D levels and normal kidney function. They will be administered cholecalciferol 50,000 IU twice weekly for 8 weeks.
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol - CKD
Other Intervention Name(s)
Vitamin D3
Intervention Description
Cholecalciferol tablet 50,000 IU twice weekly for 8 weeks
Intervention Type
Device
Intervention Name(s)
Calcitriol - CKD
Other Intervention Name(s)
1,25(OH)2D
Intervention Description
Calcitriol 0.25 mcg once daily for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol - non-CKD
Other Intervention Name(s)
Vitamin D3
Intervention Description
Cholecalciferol tablet 50,000 IU twice weekly for 8 weeks
Primary Outcome Measure Information:
Title
Monocyte Protein Expression
Description
Flow cytometry analysis of monocyte CD14, ACE, VDR, and Mac-1 expression
Time Frame
8 weeks of therapy
Title
Change in 24,25(OH)2D Levels in CKD vs. Non-CKD Subjects Receiving Cholecalciferol
Time Frame
8 weeks of therapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Chronic kidney disease w/GFR<35ml/min
Nutritional vitamin D deficiency, defined as 25(OH)D < 25ng/ml
Secondary hyperparathyroidism, PTH>75pg/mL
Exclusion Criteria:
Active infection
Recent hospitalization for acute illness (within last month)
Refusal to study participation
History of chronic inflammatory disease process (i.e. inflammatory bowel, rheumatoid arthritis, SLE, etc.)
Allergy to cholecalciferol or calcitriol
History of parathyroidectomy
Functional renal transplant within 5 years
Current treatment with immunosuppressant medications
Noncompliance with prescribed medications
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jason Stubbs, MD
Organizational Affiliation
University of Kansas Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Of Kansas Medical Center
City
Kansas City
State/Province
Kansas
ZIP/Postal Code
66160
Country
United States
12. IPD Sharing Statement
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Impact of Vitamin D Therapies on Chronic Kidney Disease
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