Viewing Study NCT00120757



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00120757
Status: COMPLETED
Last Update Posted: 2011-12-22
First Post: 2005-07-11

Brief Title: Efficacy of Alendronate Versus Placebo in the Treatment of HIV-associated Osteoporosis ANRS120
Sponsor: French National Agency for Research on AIDS and Viral Hepatitis
Organization: French National Agency for Research on AIDS and Viral Hepatitis

Study Overview

Official Title: Efficacy of Alendronate Versus Placebo in the Treatment of HIV-1 Associated Osteoporosis a Multicenter Randomized Controlled Trial ANRS 120 Fosivir
Status: COMPLETED
Status Verified Date: 2011-12
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: Osteopenia and osteoporosis are being described more frequently in people with HIV infection This study will test the efficacy of alendronate in comparison with a placebo after 2 years in people with primary osteoporosis People will receive the recommended adequate intake of calcium and vitamin D
Detailed Description: The purposes of this trial are

To study the efficacy of alendronate in HIV-associated osteoporosis
To measure the prevalence of osteoporosis in HIV patients and to detect risk factors in a large cohort of HIV patients from the screening phase

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
ANRS120 Fosivir None None None