drugset / Trial / NCT01544894

Clinical Study of Raloxifene and Strontium Ranelate in Postmenopausal Osteoporosis

NCT01544894

Phase 4 Completed 80 enrolled University of Valencia
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to compare compliance and efficacy of raloxifene and strontium ranelate in a group of women with postmenopausal osteoporosis.

Timeline

Start
2009-09
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Raloxifene Other / unclassified 60 mg
Comparator Strontium Ranelate Small molecule 2 g