NCT00634816View on ClinicalTrials.gov

Bone Mineral Density in Adult Survivors of Solid Pediatric Cancers

CompletedOBSERVATIONAL
Enrollment

38

Participants

Timeline

Start Date

April 30, 2003

Primary Completion Date

April 30, 2006

Study Completion Date

April 30, 2006

Conditions
Regional Osteoporosis as a Result of Chemotherapy
Interventions
RADIATION

DXA Scan

The patients will undergo total body, spine, proximal femoral, and forearm DEXA testing in a standardized fashion. Patients who have undergone limb surgery or irradiation to an extremity for local disease control will also undergo selected site DEXA or pQCT scanning, depending upon the site, of the affected extremity and the identical site on the contra-lateral extremity.

Trial Locations (1)

13202

SUNY Upstate Medical University, Syracuse

All Listed Sponsors
lead

State University of New York - Upstate Medical University

OTHER

NCT00634816 - Bone Mineral Density in Adult Survivors of Solid Pediatric Cancers | Biotech Hunter | Biotech Hunter