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Randomized Trial of Risedronate to Prevent Bone Loss in Renal Transplant Recipients.

This study is ongoing, but not recruiting participants.

Sponsored by: Montefiore Medical Center
Information provided by: Montefiore Medical Center
ClinicalTrials.gov Identifier: NCT00266708
  Purpose

Patients with kidney failure have underlying bone disease at the time of transplant. Fractures of various bones can be as high as 22%. Medication required for the transplant plays a role in bone loss.

Bisphosphonates are used in the general population to treat bone loss of osteoporosis and steroid-induced bone loss. While previous studies, using various bisphosphonates, have shown preservation of bone mineral density in renal transplant recipients, we have demonstrated that pamidronate, a second generation bisphosphonate, is associated with low bone turnover while still preserving bone mineral density. Improved bone mineral density is associated with decreased fracture risk in the general population, while low bone turnover may be associated with increased fracture in dialysis patients.

The purpose of this study is to determine whether risedronate, a third generation bisphosphonate, is effective in preserving bone density when given prophylactically following renal transplantation and whether it is associated with low bone turnover at one year following renal transplantation.


Condition Intervention
Renal Transplant Osteodystrophy
Drug: risedronate 35 mg weekly vs placebo

MedlinePlus related topics:   Kidney Transplantation    Minerals    Osteoporosis   

ChemIDplus related topics:   Risedronate sodium    Risedronic acid   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title:   Randomized Trial of Risedronate to Prevent Bone Loss in Renal Transplant

Further study details as provided by Montefiore Medical Center:

Primary Outcome Measures:
  • Changes in Bone Mineral Density
  • Differences in Bone turnover

Estimated Enrollment:   60
Study Start Date:   October 2002

Detailed Description:

Participants who receive a living donor kidney transplant undergo a bone biopsy at the time of kidney transplant and after one year of protocol. Once adequate kidney function is established, both groups take by mouth a weekly capsule (the control group has a placebo; the treatment group has risedronate 35 mg). Both groups undergo baseline, 6 month and 12 month DEXA bone mineral density scans. Both groups undergo bone hormonal studies at regular intervals.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Adults with end stage renal disease who are undergoing living donor kidney transplantation
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00266708

Locations
United States, New York
Montefiore Medical Center    
      Bronx, New York, United States, 10467

Sponsors and Collaborators
Montefiore Medical Center

Investigators
Principal Investigator:     Maria Coco, MD, MS     Montefiore Medical Center    
  More Information


Study ID Numbers:   02-08-224
First Received:   December 15, 2005
Last Updated:   January 12, 2007
ClinicalTrials.gov Identifier:   NCT00266708
Health Authority:   United States: Institutional Review Board

Keywords provided by Montefiore Medical Center:
renal transplant  
post-transplant osteoporosis  

Study placed in the following topic categories:
Osteoporosis
Risedronic acid

Additional relevant MeSH terms:
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Physiological Effects of Drugs
Calcium Channel Blockers
Bone Density Conservation Agents
Cardiovascular Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 20, 2008




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