drugset / Trial / NCT00398931

FLEX - Long-term Extension of FIT (Fracture Intervention Trial)(0217-051)

NCT00398931

Phase 3 Completed 1099 enrolled Organon and Co
RandomizedParallel-groupDouble-blindTreatment

Summary

This study was conducted among women who had previously received alendronate for 3 to 6 years during the Fracture Intervention Trial (FIT). Participants in the FLEX study were randomly assigned to receive alendronate (either 5 or 10 mg/day) or matching placebo during the next 5 years, in order to evaluate the effects of continuing or discontinuing alendronate treatment on bone mineral density and biochemical markers of bone turnover.

Timeline

Start
1998-02
Primary completion
2003-10
Completion
2003-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alendronic Acid Small molecule 5 mg Oral
Subject Alendronic Acid Small molecule 10 mg Oral