drugset / Trial / NCT01131884

Pilot Study of Fosamax in Spinal Cord Injury

NCT01131884

Terminated 1 enrolled University of Rochester
RandomizedParallel-groupTriple-blindPrevention

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.

Timeline

Start
2010-06
Primary completion
2012-12
Completion
2012-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Alendronic Acid Small molecule 70 mg Oral