Clinical trial

A Comparison Study With Alendronate and Raloxifene in Postmenopausal Women With…

NCT00389740 · Organon and Co, Industry · Completed

Key facts

NCT number NCT00389740
Title A Comparison Study With Alendronate and Raloxifene in Postmenopausal Women With Osteoporosis (0217-189)
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
Lead sponsor Organon and Co, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Osteoporosis, Postmenopausal
Intervention type Drug
Interventions MK0217, /Duration of Treatment : 12 Months, Comparator : raloxifene hydrochloride /Duration of Treatment : 12 Months
Enrollment 400
Start date Apr 2, 2001
Primary completion Jan 16, 2003
Completion Jan 16, 2003
First posted Oct 19, 2006
Last update posted Aug 14, 2024

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies