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Pamidronate, Vitamin D, and Calcium for the Bone Disease of Kidney and Heart Transplantation

Pamidronate, Vitamin D, and Calcium for the Bone Disease of Kidney and Heart Transplantation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00302627
Enrollment
43
Registered
2006-03-14
Start date
1999-01-31
Completion date
2002-11-30
Last updated
2018-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transplant Bone Disease

Keywords

bisphosphonates, vitamin D, calcium supplement, corticosteroid therapy, fractures

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.

Interventions

DRUGPamidronate

60mg or 90mg given at baseline, 6,12,18, and 24 months

DRUGvitamin D

baseline, 6,12 months

DRUGCalcium Carbonate

baseline, 6,12 months

Sponsors

The Heart Institute of Spokane
CollaboratorUNKNOWN
Ochsner Health System
CollaboratorOTHER
University of Washington
CollaboratorOTHER
Providence Health & Services
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Kidney or heart transplant recipients

Exclusion criteria

* Hyperparathyroidism

Design outcomes

Primary

MeasureTime frameDescription
Bone mineral density measured by dual-energy X-ray absorptiometryEvery 12 monthsPerformed at 1 year and 2 years.

Secondary

MeasureTime frameDescription
Fracture eventsEvery 6 monthsEvaluated at 6, 12, 18 months and 2 years
serum calciumEvery 6 monthsbaseline, 6,12,18 months and 2 years
parathyroid hormoneEvery 6 monthsbaseline, 6,12,18 months and 2 years
serum creatinine and estimated glomerular filtration rateEvery 6 monthsPerformed at 6,12,18 months and 2 years
proteinuriaEvery 6 monthsEvaluated at 6,12,18 months and 2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026