Viewing Study NCT00984893


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Study NCT ID: NCT00984893
Status: COMPLETED
Last Update Posted: 2016-03-04
First Post: 2009-09-23
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Intra-venous Zoledronic Acid Once Yearly
Sponsor: Novartis Pharmaceuticals
Organization:

Study Overview

Official Title: A Real-world Study Cohort of Postmenopausal Women With Osteoporosis Taking Zoledronic Acid or Oral Bisphosphonates
Status: COMPLETED
Status Verified Date: 2016-03
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: IVORY
Brief Summary: The study will assess the real life effectiveness of zoledronic acid in the management of patients with osteoporosis over 4 years of treatment. Zoledronic acid will be compared to oral bisphosphonates (OBP) with respect to the change in Bone Mineral Density (BMD) and incidence of fractures.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: