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Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation (CTX)

Primary Purpose

Heart Transplantation, Liver Transplantation, Bone Resorption

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Zoledronic acid
Alendronate
Placebo Zoledronic Acid
Placebo Alendronate
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Heart Transplantation focused on measuring Heart Transplantation, Liver Transplantation, Immunosuppression, Bone Density/drug effects, Alendronate, Zoledronic acid, Comparative study, Humans

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: A man or woman, aged 20 to 70, of any race who has had a heart or liver transplant Exclusion Criteria: hyperparathyroidism Paget's disease hyperthyroidism cancer severe kidney disease, intestinal disease active peptic ulcer disease current or past treatment for osteoporosis pregnancy or lactation severe oral/dental disease

Sites / Locations

  • Columbia University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Active Zoledronic Acid & Placebo Alendronate

Placebo Zoledronic Acid & Active Alendronate

Arm Description

Group 1 will receive an infusion of active zoledronic acid 5 mg during the first 4 weeks after transplantation. Placebo alendronate 70 mg once weekly will be initiated at the same time as the first zoledronic acid infusion.

Group 2 will receive an infusion of placebo zoledronic acid during the first 5 weeks after transplantation. Active alendronate 70 mg once weekly will be initiated at the same time as the placebo infusion.

Outcomes

Primary Outcome Measures

Percentage Change From Baseline in Total Hip Bone Mineral Density (BMD) at 12 Months
BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.

Secondary Outcome Measures

Percentage Change From Baseline in Lumbar Spine Bone Mineral Density (BMD) at 12 Months
BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.
Percentage Change From Baseline in Femoral Neck Bone Mineral Density (BMD) at 12 Months
BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.
Serum N-telopeplide Percent Change

Full Information

First Posted
February 27, 2006
Last Updated
July 18, 2018
Sponsor
Columbia University
Collaborators
Novartis Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00297830
Brief Title
Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation
Acronym
CTX
Official Title
Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
Novartis Pharmaceuticals

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the effectiveness and safety of zoledronic acid with alendronate in the prevention of bone loss after organ transplantation. Zoledronic acid is given as a single intravenous infusion. Alendronate is given as a weekly pill. Both are expected to be very effective, but it is not known which one will work best.
Detailed Description
Patients who have undergone heart or liver transplantation are usually required to remain on medications, such as Prednisone and Cyclosporine A or Tacrolimus, that prevent the body from rejecting the transplanted organ. These medications may cause bone loss which leads to thinning of the bones (osteoporosis) and therefore greatly increase the risk of having broken bones (fractures) after transplantation. Several published studies have shown that 14% to 35% of heart transplant patients develop fractures (spine, ribs and hip) during the first year after transplantation. We have previously shown that alendronate (Fosamax), a drug approved by the FDA for prevention and treatment of postmenopausal osteoporosis and prednisone-induced osteoporosis, prevents bone loss after heart transplantation. We are conducting this study to determine whether a newer drug, zoledronic acid, is as effective as alendronate. This study is a randomized, double-blind, placebo-controlled 2-year study. Participants will receive one dose of active zoledronic acid during the first month after heart or liver transplantation and weekly placebo alendronate pills or one dose of placebo zoledronic acid and weekly active alendronate pills for the first year after transplant. Over 2 years, participants will provide blood samples on nine occasions. Bone density will be performed 4-5 times and spine xrays will be performed twice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Transplantation, Liver Transplantation, Bone Resorption
Keywords
Heart Transplantation, Liver Transplantation, Immunosuppression, Bone Density/drug effects, Alendronate, Zoledronic acid, Comparative study, Humans

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
111 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active Zoledronic Acid & Placebo Alendronate
Arm Type
Experimental
Arm Description
Group 1 will receive an infusion of active zoledronic acid 5 mg during the first 4 weeks after transplantation. Placebo alendronate 70 mg once weekly will be initiated at the same time as the first zoledronic acid infusion.
Arm Title
Placebo Zoledronic Acid & Active Alendronate
Arm Type
Experimental
Arm Description
Group 2 will receive an infusion of placebo zoledronic acid during the first 5 weeks after transplantation. Active alendronate 70 mg once weekly will be initiated at the same time as the placebo infusion.
Intervention Type
Drug
Intervention Name(s)
Zoledronic acid
Other Intervention Name(s)
Zometa
Intervention Description
Drug is administered through 5 mg intravenous infusion over 20 minutes
Intervention Type
Drug
Intervention Name(s)
Alendronate
Other Intervention Name(s)
Fosamax
Intervention Description
Alendronate 70 mg will be taken once a week in the morning at least 30-60 minutes before first meal
Intervention Type
Other
Intervention Name(s)
Placebo Zoledronic Acid
Intervention Description
Infusion of placebo zoledronic acid during the first 5 weeks after transplantation
Intervention Type
Other
Intervention Name(s)
Placebo Alendronate
Intervention Description
Placebo alendronate 70 mg once weekly
Primary Outcome Measure Information:
Title
Percentage Change From Baseline in Total Hip Bone Mineral Density (BMD) at 12 Months
Description
BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.
Time Frame
Baseline, 12 months
Secondary Outcome Measure Information:
Title
Percentage Change From Baseline in Lumbar Spine Bone Mineral Density (BMD) at 12 Months
Description
BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.
Time Frame
Baseline, 12 months
Title
Percentage Change From Baseline in Femoral Neck Bone Mineral Density (BMD) at 12 Months
Description
BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.
Time Frame
Baseline, 12 months
Title
Serum N-telopeplide Percent Change
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A man or woman, aged 20 to 70, of any race who has had a heart or liver transplant Exclusion Criteria: hyperparathyroidism Paget's disease hyperthyroidism cancer severe kidney disease, intestinal disease active peptic ulcer disease current or past treatment for osteoporosis pregnancy or lactation severe oral/dental disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth Shane, M.D.
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
14973216
Citation
Shane E, Addesso V, Namerow PB, McMahon DJ, Lo SH, Staron RB, Zucker M, Pardi S, Maybaum S, Mancini D. Alendronate versus calcitriol for the prevention of bone loss after cardiac transplantation. N Engl J Med. 2004 Feb 19;350(8):767-76. doi: 10.1056/NEJMoa035617.
Results Reference
background
PubMed Identifier
23024190
Citation
Shane E, Cohen A, Stein EM, McMahon DJ, Zhang C, Young P, Pandit K, Staron RB, Verna EC, Brown R, Restaino S, Mancini D. Zoledronic acid versus alendronate for the prevention of bone loss after heart or liver transplantation. J Clin Endocrinol Metab. 2012 Dec;97(12):4481-90. doi: 10.1210/jc.2012-2804. Epub 2012 Sep 28.
Results Reference
result

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Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation

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