Viewing Study NCT00160264



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00160264
Status: COMPLETED
Last Update Posted: 2009-01-30
First Post: 2005-09-09

Brief Title: Study to Investigate if Adding Lactulose to Vitamin D and Calcium Has an Effect on the Preservation of Bone in Postmenopausal Women
Sponsor: Solvay Pharmaceuticals
Organization: Solvay Pharmaceuticals

Study Overview

Official Title: A Randomized Double-Blind Multicenter Parallel Pilot Clinical Trial to Study the Efficay of a Treatment of Lactulose Vitamin D Calcium 05 g Concurrently Controlled With a Standard Treatment Vit D Calcium in Bone Mass Preservation Among Postmenopausal Women
Status: COMPLETED
Status Verified Date: 2009-01
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 is a randomized double-blind multicentre parallel pilot clinical trial to study the efficacy of a treatment of lactulose 15 ml vitamin D 400 U calcium 05 g compared to lactulose placebo 15 ml vitamin D 400 U calcium 1 g in bone mass preservation among postmenopausal women
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