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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00594295
Other study ID # 2007-1098
Secondary ID
Status Completed
Phase N/A
First received January 3, 2008
Last updated October 1, 2015
Start date June 2007
Est. completion date July 2008

Study information

Verified date April 2010
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility 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

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin Hospitals and Clinics Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

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