Pamidronate, Vitamin D, and Calcium for the Bone Disease of Kidney and Heart Transplantation
Primary Purpose
Transplant Bone Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pamidronate
vitamin D
Calcium Carbonate
Sponsored by
About this trial
This is an interventional treatment trial for Transplant Bone Disease focused on measuring bisphosphonates, vitamin D, calcium supplement, corticosteroid therapy, fractures
Eligibility Criteria
Inclusion Criteria: Kidney or heart transplant recipients Exclusion Criteria: Hyperparathyroidism
Sites / Locations
- Providence Medical Research Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Pamidronate, Vitamin D, and Calcium
Arm Description
60mg or 90mg given at baseline, 6,12,18, and 24 months vitamin D 800 units/day calcium carbonate 1500 milligrams/day
Outcomes
Primary Outcome Measures
Bone mineral density measured by dual-energy X-ray absorptiometry
Performed at 1 year and 2 years.
Secondary Outcome Measures
Fracture events
Evaluated at 6, 12, 18 months and 2 years
serum calcium
baseline, 6,12,18 months and 2 years
parathyroid hormone
baseline, 6,12,18 months and 2 years
serum creatinine and estimated glomerular filtration rate
Performed at 6,12,18 months and 2 years
proteinuria
Evaluated at 6,12,18 months and 2 years
Full Information
NCT ID
NCT00302627
First Posted
March 10, 2006
Last Updated
August 27, 2018
Sponsor
Providence Health & Services
Collaborators
The Heart Institute of Spokane, Ochsner Health System, University of Washington
1. Study Identification
Unique Protocol Identification Number
NCT00302627
Brief Title
Pamidronate, Vitamin D, and Calcium for the Bone Disease of Kidney and Heart Transplantation
Official Title
Pamidronate, Vitamin D, and Calcium for the Bone Disease of Kidney and Heart Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
January 1999 (undefined)
Primary Completion Date
November 2002 (Actual)
Study Completion Date
November 2002 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Providence Health & Services
Collaborators
The Heart Institute of Spokane, Ochsner Health System, University of Washington
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Bone is lost rapidly and fractures occur in 10-20% of patients who receive organ transplants within 2 years. The purpose of this study is to evaluate long-term effects of a pamidronate-vitamin D-calcium regimen on bone loss, fractures, and safety in recipients of kidney and heart transplants.
Detailed Description
Pamidronate improves bone mass in numerous disorders of bone. Other bisphosphonates, as well as pamidronate, have been proven to be beneficial in steroid-related bone disorders. Steroid treatment is a major cause of bone loss after organ transplantation. Small, short-term studies suggest that pamidronate prevents bone loss in kidney and heart transplant recipients.
Many bisphosphonates cannot be used in patients with decreased kidney function. However, pamidronate can be given to these patients. This is an advantage of pamidronate in kidney and heart transplantation because of the frequent occurrence of decreased kidney function in these groups. Another advantage of pamidronate is that it is administered intravenously. Oral bisphosphonates commonly produce esophagitis, which is a challenging problem in the transplant population. Potential side-effects of pamidronate include transient hypocalcemia, lymphopenia, low-grade fever, myalgias and nausea. Recently, rare cases of proteinuria and kidney failure were reported in cancer patients receiving high-dose pamidronate. Although this side effect has not been reported in other types of patients receiving pamidronate, this is a safety concern that warrants further scrutiny in the transplant population.
In addition to bisphosphonate treatment, supplementation with calcium and vitamin D may preserve bone after organ transplantation. Prior studies have compared bisphosphonates to calcium and vitamin D regimens. However, a combination regimen including each of these treatments may preserve bone mass better than a single treatment. Data regarding treatment with a combination of a bisphosphonate, calcium, and vitamin D are lacking in kidney and heart transplantation.
Comparison(s): In a prospective, open-label, single arm trial, Pamidronate (60-90 mg) is administered within 2 weeks after kidney or heart transplant and every 6 months for 2 years. Participants are prescribed vitamin D 800 units/d or calcitriol 0.25 microgram/d if serum creatinine is greater than 2 mg/dl, and calcium carbonate 1500 mg/d.
The primary outcome is bone mineral density measured by dual-energy X-ray absorptiometry at baseline and after years 1 and 2. Fracture events and serum calcium, parathyroid hormone, creatinine, and dipstick proteinuria are also measured.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Transplant Bone Disease
Keywords
bisphosphonates, vitamin D, calcium supplement, corticosteroid therapy, fractures
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Pamidronate, Vitamin D, and Calcium
Arm Type
Experimental
Arm Description
60mg or 90mg given at baseline, 6,12,18, and 24 months
vitamin D 800 units/day
calcium carbonate 1500 milligrams/day
Intervention Type
Drug
Intervention Name(s)
Pamidronate
Other Intervention Name(s)
Transplant Bone Disease
Intervention Description
60mg or 90mg given at baseline, 6,12,18, and 24 months
Intervention Type
Drug
Intervention Name(s)
vitamin D
Other Intervention Name(s)
Vitamin D administration in Transplant
Intervention Description
baseline, 6,12 months
Intervention Type
Drug
Intervention Name(s)
Calcium Carbonate
Other Intervention Name(s)
Calcium administration in Transplant
Intervention Description
baseline, 6,12 months
Primary Outcome Measure Information:
Title
Bone mineral density measured by dual-energy X-ray absorptiometry
Description
Performed at 1 year and 2 years.
Time Frame
Every 12 months
Secondary Outcome Measure Information:
Title
Fracture events
Description
Evaluated at 6, 12, 18 months and 2 years
Time Frame
Every 6 months
Title
serum calcium
Description
baseline, 6,12,18 months and 2 years
Time Frame
Every 6 months
Title
parathyroid hormone
Description
baseline, 6,12,18 months and 2 years
Time Frame
Every 6 months
Title
serum creatinine and estimated glomerular filtration rate
Description
Performed at 6,12,18 months and 2 years
Time Frame
Every 6 months
Title
proteinuria
Description
Evaluated at 6,12,18 months and 2 years
Time Frame
Every 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Kidney or heart transplant recipients
Exclusion Criteria:
Hyperparathyroidism
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katherine R. Tuttle, MD,FASN,FACP
Organizational Affiliation
Providence Medical Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Providence Medical Research Center
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Pamidronate, Vitamin D, and Calcium for the Bone Disease of Kidney and Heart Transplantation
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