drugset / Trial / NCT05325515

The Effect of Effervescent Alendronate on Bone Turnover

NCT05325515

Phase 4 Completed 64 enrolled Aarhus University Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

64 postmenopausal women are randomized to treatment with either effervescent and buffered alendronate or conventional alendronate -both 70mg weekly for 16 weeks to see if bone turnover is suppressed to the same extent as in the conventional formulation with the effervescent form.

Timeline

Start
2021-10-01
Primary completion
2022-09-01
Completion
2022-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Alendronic Acid Small molecule 70 mg

Indications