POWER Point of Care Effect on Satisfaction of Treatment

Status Completed

Clinical Trial Summary

To compare the subject satisfaction rating in women treated for postmenopausal osteoporosis with Actonel 35mg Once-a-Week for 24 weeks, and receiving feedback information, after 12 weeks of treatment, based on bone resorption marker results using the NTx Point-Of-Care (POC) device, to similar women treated as per regular clinical practice

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Osteoporosis, Postmenopausal

Clinical Trial Details

NCT number	NCT00549068
Study type	Interventional
Source	Sanofi
Contact
Status	Completed
Phase	Phase 4
Start date	February 2003
Completion date	November 2004

View Details

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