drugset / Trial / NCT00259857

Safety and Efficacy of Alendronate (Fosamax) in Children With Osteoporosis

NCT00259857

RandomizedCrossoverDouble-blindTreatment

Summary

We have previously evaluated the safety and efficacy of Alendronate in 10 patients with juvenile osteoporosis during a 12-month clinical trial. We have documented that Alendronate improved BMD of the spine and hip without any major side effects. There were no additional fractures during therapy. The present study is designed to further evaluate the safety and efficacy of Alendronate in 20 children with juvenile osteoporosis using a double-blind, randomized, placebo-controlled, cross-over protocol.

Timeline

Start
2003-10
Primary completion
2008-03
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Alendronic Acid Small molecule 35 mg Oral
Subject Alendronic Acid Small molecule 70 mg Oral

Indications