drugset / Trial / NCT02616744

Study of Oral Bisphosphonate for Osteopenic Women Treated With Adjuvant Aromatase Inhibitors

NCT02616744

Phase 2 Completed 171 enrolled Careggi University Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

A single--blind, randomized, placebo--controlled phase II study to evaluate the impact of oral bisphosphonate treatment on bone mineral density in osteopenic women receiving aromatase inhibitors as adjuvant treatment.

Timeline

Start
2011-01
Primary completion
2016-05
Completion
2016-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Ibandronic acid Unknown 150 mg Oral

Indications