- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00558948
Musculoskeletal Outcomes After Bone Marrow Transplant
August 18, 2009 updated by: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
The purpose of the study is to evaluate bone mineral density and muscle strength in survivors of bone marrow transplant.
Association with age, type of transplant, steroids, years since transplant, body composition, endocrinopathies, radiation, quality of life and physical activity will be explored.
Study Overview
Status
Completed
Detailed Description
Bone marrow transplant survivors are at risk of diminished bone mineral density.
Mechanisms and risks are not well understood.
This study will help identify risks factors for developing this complication.
Study Type
Observational
Enrollment (Actual)
48
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Maryland
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Baltimore, Maryland, United States, 21212
- Johns Hopkins University, Bayview Campus
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
8 years to 30 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Survivors of bone marrow transplant (autologous and allogeneic) who are at least 1 year from transplant.
Description
Inclusion Criteria:
- Ages 8-30 years
- One year from transplant
Exclusion Criteria:
- No current steroid use
- Medical conditions that would prohibit testing
- Neuropsychological conditions that prohibit completing questionnaires
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Kathy Ruble, PhDc, RN, Johns Hopkins university, School of Nursing
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2007
Primary Completion (Actual)
August 1, 2009
Study Completion (Actual)
August 1, 2009
Study Registration Dates
First Submitted
November 14, 2007
First Submitted That Met QC Criteria
November 15, 2007
First Posted (Estimate)
November 16, 2007
Study Record Updates
Last Update Posted (Estimate)
August 19, 2009
Last Update Submitted That Met QC Criteria
August 18, 2009
Last Verified
August 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- J06120
- 1F31NR010038-01 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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