2,456
Participants
Start Date
May 31, 2005
Primary Completion Date
November 30, 2009
Study Completion Date
November 30, 2009
Zoledronic Acid
Zoledronic Acid 5 mg in 100 mL physiologic 0.9% normal saline for intravenous infusion.
Placebo
100 mL physiologic 0.9% normal saline for intravenous infusion.
Winthrop U Hospital, Mineola
University of Pittsburgh, Pittsburgh
Thomas Jefferson University Hospital, Philadelphia
Radiant Research, Wyomissing
Osteoporosis Clinical Trial Center, Hagerstown
McGuire Veterans Affairs Medical Center, Richmond
VA Commonwealth University, Richmond
United Osteoporosis Centers (UOC), Gainesville
CRIA Research, Fort Lauderdale
Comprehensive Clinical Trials, LLC, West Palm Beach
Radiant Research, Stuart
University of Tennessee Health Science, Memphis
University of Cincinnati Bone Health and Osteoporosis Center, Cincinnati
School of Medicine, Indianapolis
Medical Specialist Clinical Research Center, Munster
Odyssey Research Services/CCRC Internal Medical, Fargo
Northwestern University Center for Clinical Research, Chicago
Washington University Center for Clinical Studies, St Louis
Heartland Research Associates, LLC, Wichita
University of Arkansas for Medical Science, Little Rock
Colorado Center for Bone Research, Lakewood
Southern Arizona VA, Tucson
New Mexico Clinical Research and Osteoporosis Center Inc, Albuquerque
Osteoporosis Medical Center, Beverly Hills
Osteoporosis Prevention Center, San Diego
Diablo Clinical Research, Inc, Walnut Creek
Puget Sound Osteoporosis Center, Seattle
Maine Center for Osteoporosis Research and Education, Bangor
Clinical Pharmacology Study Groups, Worcester
Rhode Island Hospital, Endocrinology Clinical Research Unit, Providence
Novartis, Nuremberg
Lead Sponsor
Novartis
INDUSTRY