drugset / Trial / NCT00010439

Phase II Study of Alendronate Sodium in Children With High-Turnover Idiopathic Juvenile Osteoporosis

NCT00010439

Non-randomizedSingle-groupOpen-labelTreatment

Summary

OBJECTIVES: I. Determine the effects of alendronate sodium on skeletal remodeling and bone mineral density of the hip and spine in children with high-turnover idiopathic juvenile osteoporosis.

Timeline

Start
2000-09
Primary completion
2003-10
Completion
2008-11

Drugs

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

Indications