Overview

Pilot Study of Fosamax in Spinal Cord Injury

Status:
Terminated
Trial end date:
2012-12-01
Target enrollment:
Participant gender:
Summary
Study is designed to evaluate the efficacy of oral fosamax in prevention on osteoporosis in acute spinal cord injury. Efficacy will be measured by a duel energy X-Ray absorptiometry (DEXA) scan every 6 months. Patients will complete 3 visits, screening, 6 months, 12 months and be required to take oral fosamax versus placebo weekly.
Phase:
N/A
Details
Lead Sponsor:
University of Rochester
Treatments:
Alendronate