Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease
Primary Purpose
End-Stage Renal Disease
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cholecalciferol
Sponsored by
About this trial
This is an interventional treatment trial for End-Stage Renal Disease focused on measuring Endstage renal disease, Vitamin D, Monocyte function
Eligibility Criteria
Inclusion Criteria:
- End-stage renal disease undergoing maintenance hemodialysis at KUMC outpatient hemodialysis unit
- Dialysis vintage of at least 6 months duration
- Nutritional vitamin D deficiency, defined as 25(OH)D <25 ng/ml
- Age 21 to 88 years
Exclusion Criteria:
- Active infection
- Recent hospitalization for acute illness (within last 1 month)
- Refusal to study participation
- Poorly controlled secondary hyperparathyroidism (iPTH>500)
- History of chronic inflammatory disease process, such as inflammatory bowel, rheumatoid arthritis, lupus, etc.
- Cinacalcet therapy
- Previous allergy to ergocalciferol
- History of parathyroidectomy
- Current treatment with immunosuppressant medications
- Noncompliance with prescribed hemodialysis regimen (i.e. skipping treatments, ending sessions early)
- Functional renal transplant within the last five years
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
Cholecalciferol (Vitamin D)
Outcomes
Primary Outcome Measures
Change in Monocyte VDR Expression With Vitamin D Therapy
Monocytes will be analyzed pre- and post-cholecalciferol by flow cytometry to measure changes in monocyte VDR expression. Unit of measure is represented by mean florescence intensity (MFI), which is a relative measure.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00677534
Brief Title
Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease
Official Title
Exploring the Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
August 2009 (Actual)
Study Completion Date
August 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Kansas
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this study is to evaluate the role of nutritional Vitamin D deficiency as a potential contributor to the morbidity witnessed in patients with end-stage renal disease
Detailed Description
The goals of this study are to elucidate the function of extrarenal 1 alpha-hydroxylase activity in the setting of renal failure and to evaluate the role of nutritional vitamin D deficiency as a potential contributor to monocyte-associated inflammatory pathways in patients with end-stage renal disease (ESRD). This study will consist of patients on chronic maintenance hemodialysis three times per week who have been identified to have nutritional vitamin D deficiency. After consent for study enrollment, patients will undergo a 4 week washout period of all active vitamin D supplementation. After washout is complete, an blood sample will be obtained for baseline 25(OH)D levels and monocyte isolation for analysis by flow cytometry. Patients will then be started on cholecalciferol 50,000 IU twice weekly for 8 weeks. 25-vitamin D levels will be monitored midway through the treatment phase of the study and dosing adjusted as further described in detail within the protocol section. An additional blood sample will be drawn post-therapy for repeat 25(OH)D levels and monocyte isolation for flow cytometry analysis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-Stage Renal Disease
Keywords
Endstage renal disease, Vitamin D, Monocyte function
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Cholecalciferol (Vitamin D)
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol
Other Intervention Name(s)
Vitamin D, ergocalciferol
Intervention Description
50,000 Units PO Twice weekly for 8 weeks
Primary Outcome Measure Information:
Title
Change in Monocyte VDR Expression With Vitamin D Therapy
Description
Monocytes will be analyzed pre- and post-cholecalciferol by flow cytometry to measure changes in monocyte VDR expression. Unit of measure is represented by mean florescence intensity (MFI), which is a relative measure.
Time Frame
Change from End of Washout to Week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
88 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
End-stage renal disease undergoing maintenance hemodialysis at KUMC outpatient hemodialysis unit
Dialysis vintage of at least 6 months duration
Nutritional vitamin D deficiency, defined as 25(OH)D <25 ng/ml
Age 21 to 88 years
Exclusion Criteria:
Active infection
Recent hospitalization for acute illness (within last 1 month)
Refusal to study participation
Poorly controlled secondary hyperparathyroidism (iPTH>500)
History of chronic inflammatory disease process, such as inflammatory bowel, rheumatoid arthritis, lupus, etc.
Cinacalcet therapy
Previous allergy to ergocalciferol
History of parathyroidectomy
Current treatment with immunosuppressant medications
Noncompliance with prescribed hemodialysis regimen (i.e. skipping treatments, ending sessions early)
Functional renal transplant within the last five years
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
12. IPD Sharing Statement
Citations:
PubMed Identifier
20007751
Citation
Stubbs JR, Idiculla A, Slusser J, Menard R, Quarles LD. Cholecalciferol supplementation alters calcitriol-responsive monocyte proteins and decreases inflammatory cytokines in ESRD. J Am Soc Nephrol. 2010 Feb;21(2):353-61. doi: 10.1681/ASN.2009040451. Epub 2009 Dec 10.
Results Reference
result
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Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease
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