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The Role of Vitamin D in Immune Function in Patients With Chronic Kidney Disease (CKD) Stages 3 and 4.

Primary Purpose

Chronic Kidney Disease

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
cholecalciferol
doxercalciferol
placebo
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Chronic Kidney Disease focused on measuring vitamin D, determine, normal, intrapatient, interpatient, variability, measures, immune system

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • no administration of any form of vitamin D supplement or therapy in the last 60 days except for that in a multi vitamin
  • Hgb >10 mg/dl
  • able to sign informed consent
  • CKD stage 3 (GFR 30-59ml/min) or stage 4 (GFR 15-29ml/min)
  • iPTH <70pg/ml for stage 3 or iPTH <110pg/ml for stage 4
  • calcidiol levels < or +20ng/ml

Exclusion Criteria:

  • initial corrected Calcium >9.7mg/dl
  • initial serum Phosphorus >5.0mg/dl
  • initial standardized blood pressure of >160/100
  • history of significant liver disease or cirrhosis
  • anticipated requirement for dialysis in 6 months
  • malabsorption, severe chronic diarrhea, or ileostomy
  • no calcimimetic or active vitamin D therapy 60 days prior to enrollment

Sites / Locations

  • Indiana University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

1

2

3

Arm Description

4000 IU of cholecalciferol per day

1 mcg of doxercalciferol per day.

placebo for six months

Outcomes

Primary Outcome Measures

The primary endpoint will be the change in CD4+/CD8+ ratio and other flow cytometry parameters based on the results of Aims 1 and 2, TH1/TH2 cytokine profile, and conversion from anergic to reactive skin testing.

Secondary Outcome Measures

A change in mean blood pressure from one week of ambulatory measures, random protein/creatinine ratio, and differences in muscle strength by timed up and go test, and measures of quality of life using the SF36 forms.

Full Information

First Posted
September 8, 2008
Last Updated
March 28, 2013
Sponsor
Indiana University
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1. Study Identification

Unique Protocol Identification Number
NCT00749736
Brief Title
The Role of Vitamin D in Immune Function in Patients With Chronic Kidney Disease (CKD) Stages 3 and 4.
Official Title
The Role of Vitamin D in Immune Function in Patients With CKD Stages 3 and 4.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2013
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Indiana University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients with chronic kidney disease (CKD) are commonly deficient in vitamin D, with low levels of both calcidiol (25 hydroxy vitamin D) and calcitriol (1,25-hydroxy vitamin D). Patients with CKD are also known to have abnormalities in their immune cells, increased susceptibility to infection and increased prevalence of malignancies. In patients without kidney disease, repletion of vitamin D appears to help some immune mediated diseases. Thus it is logical that patients with CKD who are vitamin D deficient may benefit from repletion of vitamin D, in either its native form (cholecalciferol/ergocalciferol) or in the form of calcitriol or its analogues. However, no interventional data demonstrates that repletion positively impacts immune status in CKD patients. To test this hypothesis, a large interventional study will be required. However, prior to conducting this study, several important steps are needed. The present proposal aims to generate the necessary data to appropriately plan and conduct a future multi center interventional study. Specifically, we will examine the following specific aims in a population of CKD stage 3 and 4 subjects from Indiana University Affiliated Nephrology Clinics and determine if abnormalities in immune cells and immune blood tests are related to abnormalities in vitamin D. how reproducible these changes are on repeat testing and if repletion of vitamin D changes these cells and immune blood tests in a small pilot study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease
Keywords
vitamin D, determine, normal, intrapatient, interpatient, variability, measures, immune system

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
4000 IU of cholecalciferol per day
Arm Title
2
Arm Type
Active Comparator
Arm Description
1 mcg of doxercalciferol per day.
Arm Title
3
Arm Type
Placebo Comparator
Arm Description
placebo for six months
Intervention Type
Dietary Supplement
Intervention Name(s)
cholecalciferol
Intervention Description
4000 IU of cholecalciferol per day 15 patients will be enrolled in each arm.
Intervention Type
Dietary Supplement
Intervention Name(s)
doxercalciferol
Intervention Description
1 mcg of doxercalciferol per day
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Intervention Description
placebo for 6 months; with stratification based on stage of CKD by modified MDRD formula. 15 patients will be enrolled in each arm.
Primary Outcome Measure Information:
Title
The primary endpoint will be the change in CD4+/CD8+ ratio and other flow cytometry parameters based on the results of Aims 1 and 2, TH1/TH2 cytokine profile, and conversion from anergic to reactive skin testing.
Time Frame
6 months from baseline visit
Secondary Outcome Measure Information:
Title
A change in mean blood pressure from one week of ambulatory measures, random protein/creatinine ratio, and differences in muscle strength by timed up and go test, and measures of quality of life using the SF36 forms.
Time Frame
6 months from baseline visit.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: no administration of any form of vitamin D supplement or therapy in the last 60 days except for that in a multi vitamin Hgb >10 mg/dl able to sign informed consent CKD stage 3 (GFR 30-59ml/min) or stage 4 (GFR 15-29ml/min) iPTH <70pg/ml for stage 3 or iPTH <110pg/ml for stage 4 calcidiol levels < or +20ng/ml Exclusion Criteria: initial corrected Calcium >9.7mg/dl initial serum Phosphorus >5.0mg/dl initial standardized blood pressure of >160/100 history of significant liver disease or cirrhosis anticipated requirement for dialysis in 6 months malabsorption, severe chronic diarrhea, or ileostomy no calcimimetic or active vitamin D therapy 60 days prior to enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sharon M Moe, MD
Organizational Affiliation
Indiana University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indiana University School of Medicine
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Role of Vitamin D in Immune Function in Patients With Chronic Kidney Disease (CKD) Stages 3 and 4.

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