Osteoporosis Prevention With Low Dose Alendronate

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of the intermittent administration of alendronate in a low dose, 70 mg once every two week, as osteoporosis prevention for menopausal, osteopenic patients, who don't want or can't receive an oestrogenic substitution treatment.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Osteopenia

Clinical Trial Details

NCT number	NCT00463268
Study type	Interventional
Source	University Hospital of Mont-Godinne
Contact
Status	Completed
Phase	Phase 3
Start date	September 2007
Completion date	January 2012

View Details

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