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Follow-up of Bone Quality in Long-Term Bone Marrow Transplant Survivors

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00594295
First Posted: January 15, 2008
Last Update Posted: October 5, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University of Wisconsin, Madison
  Purpose
Brittle and broken bones can occur after organ transplantation. However, the long-term effects of bone marrow transplantation on bone health and the risk of breaking bones are not well understood. This study will help to assess how common it is for those who have received a bone marrow transplant to have fractures. It will also investigate blood tests related to bone health. This will be done by measuring bone mineral density and obtaining blood tests.

Condition
Osteoporotic Fractures

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Follow-up of Bone Quality in Long-Term Bone Marrow Transplant Survivors

Resource links provided by NLM:


Further study details as provided by University of Wisconsin, Madison:

Biospecimen Retention:   Samples Without DNA
whole blood, serum

Estimated Enrollment: 15
Study Start Date: June 2007
Study Completion Date: July 2008
Primary Completion Date: July 2008 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Bone marrow transplant patients at least 6 years post transplant
Criteria

Inclusion Criteria:

  • Participation in the initial "Assessment of skeletal status following allogeneic bone marrow transplantation" Study (HSC97-632-408).
  • Able and willing to sign informed consent.

Exclusion Criteria:

  • All of the contacted long-term BMT survivors that are willing to participate will be included in this study
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00594295


Locations
United States, Wisconsin
University of Wisconsin Hospitals and Clinics
Madison, Wisconsin, United States, 53705
Sponsors and Collaborators
University of Wisconsin, Madison
Investigators
Principal Investigator: Neil C Binkley, MD University of Wisconsin - Institute on Aging
  More Information

Responsible Party: University of Wisconsin, Madison
ClinicalTrials.gov Identifier: NCT00594295     History of Changes
Other Study ID Numbers: 2007-1098
First Submitted: January 3, 2008
First Posted: January 15, 2008
Last Update Posted: October 5, 2015
Last Verified: April 2010

Additional relevant MeSH terms:
Osteoporotic Fractures
Fractures, Bone
Wounds and Injuries