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How Bone is Made in Children Receiving Dialysis

Primary Purpose

Bone Mineralization Defect

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Vitamin D2
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bone Mineralization Defect

Eligibility Criteria

6 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • medically stable patients
  • 6-21 years old
  • undergoing treatment with continuous cycling peritoneal dialysis
  • evidence of mineralization defect and secondary hyperparathyroidism

Exclusion Criteria:

  • histopathological lesion of bone such as adynamic bone or osteomalacia
  • poor compliance
  • current treatment with prednisone or other immunosuppressives
  • treatment with human recombinant growth hormone
  • parathyroidectomy

Sites / Locations

  • Loma Linda UniversityRecruiting
  • Childrens Hospital Los AngelesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Treatment with vitamin D2

Standard of Care

Arm Description

Vitamin D2 50,000u titrated to serum 25(OH)D values given orally once a month in addition to standard of care: Doxercalciferol escalating doses beginning at 2.5 mcg given orally thrice weekly. Sevelamer Carbonate 800 mg (1600- 4800 mg) given orally with each meal

Standard of Care: Doxercalciferol escalating doses beginning at 2.5 mcg given orally thrice weekly. Sevelamer Carbonate 800 mg (1600- 4800 mg) given orally with each meal

Outcomes

Primary Outcome Measures

Improvement of bone mineralization defect demonstrated by bone histomorphometry
Iliac crest bone biopsy pre and post treatment with vitamin D2

Secondary Outcome Measures

Radiographic improvement of skeletal abnormalities associated with renal osteodystrophy
We will compare skeletal lesions identified through radiographic studies with bone histomorphometry pre and post treatment with vitamin D2

Full Information

First Posted
February 20, 2013
Last Updated
February 22, 2013
Sponsor
University of California, Los Angeles
Collaborators
Children's Hospital Los Angeles, Loma Linda University, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT01799317
Brief Title
How Bone is Made in Children Receiving Dialysis
Official Title
Regulation of Bone Mineralization in Renal Osteodystrophy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Unknown status
Study Start Date
March 2009 (undefined)
Primary Completion Date
June 2014 (Anticipated)
Study Completion Date
June 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
Children's Hospital Los Angeles, Loma Linda University, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study outlined is designed to measure and to determine whether the combined use of vitamin D2 (ergocalciferoI) and 1-alpha-hydroxyvitamin D2 (doxercalciferol)) or doxercalciferol alone will correct the mineralization defect in pediatric patients with established secondary hyperparathyroidism (2°HPT) undergoing regular peritoneal dialysis. Serum phosphorus levels will be controlled with a calcium¬-free-metal free phosphate binder; (obtained at baseline and after 8 months of treatment) sevelamer. Indices of bone mineralization obtained at baseline and after 8 months of treatment will be measured by quantitative histomorphometry in iliac crest bone biopsies after double tetracycline labeling. Immunohistochemistry will be done in specimens of bone biopsies from iliac crest to examine the expression for selected markers of bone turnover and mineralization such as FGF-23, DMP1, MEPE and OPG. Serum PTH levels will be measured with the 1st and 2nd generation immunometric assay (PTH-IMAs) and fibroblast growth factor-23 (FGF-23) will be determined by one assay with specific detection antibodies that are against epitopes within the C-terminus of FGF-23 and another assay that uses antibodies against epitopes within the N- and C-terminal portions of the molecule respectively. The value of non-invasive assessment of bone mass by quantitative computed tomography (QCT) and its relationship with vascular disease determined by ultrasound (US) of intimal carotid thickness (CIMT) will be correlated with bone histomorphometry and the different biochemical determinations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Mineralization Defect

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment with vitamin D2
Arm Type
Active Comparator
Arm Description
Vitamin D2 50,000u titrated to serum 25(OH)D values given orally once a month in addition to standard of care: Doxercalciferol escalating doses beginning at 2.5 mcg given orally thrice weekly. Sevelamer Carbonate 800 mg (1600- 4800 mg) given orally with each meal
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Standard of Care: Doxercalciferol escalating doses beginning at 2.5 mcg given orally thrice weekly. Sevelamer Carbonate 800 mg (1600- 4800 mg) given orally with each meal
Intervention Type
Drug
Intervention Name(s)
Vitamin D2
Other Intervention Name(s)
Ergocalciferol
Intervention Description
These patients will receive standard of care vitamin D 1,25 therapy with intervention of vitamin D2
Primary Outcome Measure Information:
Title
Improvement of bone mineralization defect demonstrated by bone histomorphometry
Description
Iliac crest bone biopsy pre and post treatment with vitamin D2
Time Frame
8 months
Secondary Outcome Measure Information:
Title
Radiographic improvement of skeletal abnormalities associated with renal osteodystrophy
Description
We will compare skeletal lesions identified through radiographic studies with bone histomorphometry pre and post treatment with vitamin D2
Time Frame
8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: medically stable patients 6-21 years old undergoing treatment with continuous cycling peritoneal dialysis evidence of mineralization defect and secondary hyperparathyroidism Exclusion Criteria: histopathological lesion of bone such as adynamic bone or osteomalacia poor compliance current treatment with prednisone or other immunosuppressives treatment with human recombinant growth hormone parathyroidectomy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Isidro Salusky, MD
Phone
310.206.6987
Email
isalusky@mednet.ucla.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isidro Salusky, MD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loma Linda University
City
Loma Linda
State/Province
California
ZIP/Postal Code
92354
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shobbha Sahney, MD
Phone
909-558-8242
Email
ssahney@llu.edu
First Name & Middle Initial & Last Name & Degree
Shobha Sahney, MD
Facility Name
Childrens Hospital Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kevin Lemley, MD
Phone
323-361-2295
Email
klemley@chla.usc.edu
First Name & Middle Initial & Last Name & Degree
Kevin Lemley, MD

12. IPD Sharing Statement

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How Bone is Made in Children Receiving Dialysis

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