Viewing Study NCT00431444



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Last Modification Date: 2024-10-26 @ 9:30 AM
Study NCT ID: NCT00431444
Status: COMPLETED
Last Update Posted: 2011-03-29
First Post: 2007-02-01

Brief Title: Effects of Zoledronic Acid and Raloxifene on Bone Turnover Markers in Postmenopausal Women With Low Bone Mineral Density
Sponsor: Novartis
Organization: Novartis

Study Overview

Official Title: A Multi-center Randomized Double-blind Double-dummy Study in Postmenopausal Women With Low Bone Mineral Density to Compare the Effects of a Single Dose of iv Zoledronic Acid 5 mg With Daily Oral Raloxifene 60 mg OD on Bone Turnover Markers
Status: COMPLETED
Status Verified Date: 2011-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study will compare the effects of Zoledronic acid and Raloxifene in reducing bone turnover markers in postmenopausal women with low bone mineral density over 6 months
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None