Viewing Study NCT00389740



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Last Modification Date: 2024-10-26 @ 9:28 AM
Study NCT ID: NCT00389740
Status: COMPLETED
Last Update Posted: 2022-02-03
First Post: 2006-10-18

Brief Title: A Comparison Study With Alendronate and Raloxifene in Postmenopausal Women With Osteoporosis 0217-189
Sponsor: Organon and Co
Organization: Organon and Co

Study Overview

Official Title: A Randomized Double-Blind Double-Dummy Parallel-Group Multicenter Study to Evaluate and Compare the Effects of Alendronate and Raloxifene on Bone Mineral Density in Postmenopausal Women With Osteoporosis
Status: COMPLETED
Status Verified Date: 2022-02
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: The purpose of this study is to compare how well alendronate and raloxifene increase the bone density in women who have osteoporosis and have experienced menopause
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
Secondary IDs
Secondary ID Type Domain Link
2006_537 None None None