Safety and Effects of Supplementation With Ergocalciferol on Erythropoietin Dosing in Hemodialysis Patients

Phase 4

Completed

• Conditions: End Stage Renal Disease
• Interventions: Dietary Supplement: ergocalciferol supplementation; Other: placebo

• Registration Number: NCT01395823
• Lead Sponsor: Dialysis Clinic, Inc.

Brief Summary

A few studies have reported erythropoiesis-stimulating agent (ESA) doses before and after 25D supplementation, but only one of these is a prospective clinical trial, and it is a small, single center study lacking a control arm. The investigators propose to conduct a double blind, randomized, placebo controlled clinical trial of ergocalciferol supplementation to confirm safety and determine effects on Erythropoietin (EPO) dosing, active D dosing, and mineral metabolic parameters in hemodialysis patients.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-06
• Study First Submitted: 2011-07-14
• Study First Submitted QC: 2011-07-15
• Study First Posted: 2011-07-18
• Primary Completion: 2014-04
• Study Completion: 2015-06
• Results First Submitted: 2016-01-08
• Status Verified: 2016-02
• Results First Submitted QC: 2016-02-15
• Last Update Submitted: 2016-02-15
• Results First Posted: 2016-03-14
• Last Update Posted: 2016-03-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 470

Inclusion Criteria

1. Patients treated with thrice weekly in-center hemodialysis (HD) for more than 90 days.
2. Treated with EPO for at least 90 days. The mode of administration, intravenous (IV) or subcutaneous (SC), must remain the same for 90 days prior to enrollment.
3. The method by which EPO is prescribed (per DCI Corporate or local protocol or per physician on an individualized basis) must remain the same for at least 90 days prior to enrollment with respect to the ceiling for the total EPO dose administered per week, if a ceiling is used, and the level of hemoglobin (Hgb) at which EPO is discontinued (Hgb cutoff), if a Hgb cutoff is used.
4. The method by which IV Iron is prescribed (per DCI Corporate or local protocol or per physician on an individualized basis) must remain the same for at least 90 days prior to enrollment with respect to the serum ferritin and transferrin saturation (TSAT) targeted, if specific ferritin and TSAT targets are used

Exclusion Criteria

1. Patients with a serum calcium ≥10.5 mg/dL on at least one occasion in the past 30 days.
2. Patients with a serum phosphorus >8.0 mg/dL on at least one occasion in the past 30 days.
3. Active infection defined by the use of IV antibiotic use within the past 30 days.
4. Current use of immunosuppressant medications other than low dose corticosteroids (prednisone <10 mg per day or equivalent)
5. History of a hematological malignancy (e.g. multiple myeloma, leukemia).
6. Sickle cell disease (sickle cell trait is not an exclusion).
7. Myelodysplasia requiring 1 or more blood transfusions in the past 3 months.
8. Transfusion for any reason within the past 30 days.
9. Medical conditions that cause a reduction in the absorption of oral vitamin D including Crohn's disease, celiac sprue, cystic fibrosis and surgical removal of part or all of the stomach or intestine.
10. Medications that cause a reduction in the absorption of oral vitamin D including cholestyramine (Questran, others), colestipol (Colestid, others) and orlistat (Xenical, Alli).
11. Known allergy/adverse reaction to ergocalciferol.
12. Treated with ergocalciferol and/or cholecalciferol (except if part of a multi-vitamin) within the last 3 months.
13. Average Kt/V < 1.3 on past three monthly labs. There must be at least 2 monthly Kt/V values in the past three months.
14. Skipped more than 3 dialysis treatments (excluding planned missed treatments) within the past 3 months for reasons other than hospitalization.
15. Life expectancy less than 6 months.
16. Kidney transplantation planned in the next 6 months.
17. Switch to peritoneal dialysis planned in the next 6 months.
18. Pregnant or planning to become pregnant within the next 6 months. A pre-menopausal woman must agree to use contraception for the duration of the study. If a woman has not had menses in over 12 months, consider this patient to be menopausal.
19. Unable or unwilling to give informed consent.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
ergocalciferol supplementation	ergocalciferol supplementation	-
placebo	placebo	-

Primary Outcome Measures

Name	Time	Method
EPO Dose	Baseline, 6 months	The primary outcome is the change in the median EPO dose from baseline to 6 months after ergocalciferol supplementation.

Trial Locations

Locations (12)

DCI - Shreveport; 🇺🇸 Shreveport, Louisiana, United States

DCI - New Brunswick; 🇺🇸 New Brunswick, New Jersey, United States

DCI- Omaha; 🇺🇸 Omaha, Nebraska, United States

DCI - North Brunswick; 🇺🇸 North Brunswick, New Jersey, United States

DCI - Boston; 🇺🇸 Boston, Massachusetts, United States

DCI - Albany; 🇺🇸 Albany, Georgia, United States

DCI - Redding; 🇺🇸 Redding, California, United States

DCI - Kansas City; 🇺🇸 Kansas City, Missouri, United States

DCI - Philadelphia; 🇺🇸 Philadelphia, Pennsylvania, United States

DCI- Columbia; 🇺🇸 Columbia, Missouri, United States

DCI - Knoxville; 🇺🇸 Knoxville, Tennessee, United States

DCI - Maryville; 🇺🇸 Maryville, Tennessee, United States