drugset / Trial / NCT00271713

Impact of Oral Ibandronate 150 mg Monthly on Structural Properties of Bone in Postmenopausal Osteoporosis (SPIMOS-3D)

NCT00271713

Phase 4 Completed 70 enrolled Charite University, Berlin, Germany
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Efficacy: To investigate changes of structural bone properties in vivo using 3DpQCT ("Xtreme" CT, Scanco) in monthly oral ibandronate therapy for women with postmenopausal osteoporosis. Major structural bone parameters which determine bone strength and predict fracture risk earlier and more precisely are measurable in vivo by 3DpQCT. Safety: To assess the tolerability and safety of ibandronate therapy

Timeline

Start
2006-03
Primary completion
2007-09
Completion
2007-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ibandronate Other / unclassified 150 mg Oral
Comparator Calcium carbonate Other / unclassified 500 mg
Comparator Vitamin D Other / unclassified 800 iu