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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00049829
Other study ID # CZOL446H2301
Secondary ID
Status Completed
Phase Phase 3
First received November 14, 2002
Last updated November 1, 2011
Start date January 2002

Study information

Verified date November 2011
Source Novartis
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

HORIZON-PFT (Pivotal Fracture Trial) will study the effect of zoledronic acid, given once per year, on the treatment of osteoporosis in women past menopause. Hip and vertebral fractures are the most devastating consequences of osteoporosis. HORIZON-PFT is designed to determine the benefits of zoledronic acid in fracture reduction at both the hip and spine.


Recruitment information / eligibility

Status Completed
Enrollment 7700
Est. completion date
Est. primary completion date June 2006
Accepts healthy volunteers No
Gender Female
Age group 65 Years to 89 Years
Eligibility Inclusion Criteria:

- Female, 65-89 years old

- No history of severe liver, kidney or eye disease

Exclusion Criteria:

- Current bisphosphonate users such as Aredia® (pamidronate), Didronel® (etidronate), Fosamax® (alendronate), Actonel® (risedronate), Skelid® (tiludronate)

- Using hip protectors

Other protocol-defined inclusion/exclusion criteria may apply.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Zoledronic Acid


Locations

Country Name City State
Germany Novartis Nuernberg
United States New Mexico Clinical Research and Osteoporosis Center, Inc Albuquerque New Mexico
United States Maine Center for Osteoporosis Research and Education Bangor Maine
United States Osteoporosis Medical Center Beverly Hills California
United States University of Alabama at Birmingham Birmingham Alabama
United States Brigham and Women's Hospital Boston Massachusetts
United States Northwestern University Center for Clinical Research Chicago Illinois
United States University of Cincinnati Bone Health and Osteoporosis Center Cincinnati Ohio
United States Cleveland Clinic Foundation Cleveland Ohio
United States Altoona Center for Clinical Research Duncansville Pennsylvania
United States Center for Arthritis and Osteoporosis Elizabethtown Kentucky
United States Endwell Family Physicians Endwell New York
United States Internal Medicine Associates Fargo North Dakota
United States CRA Research Ft. Lauderdale Florida
United States United Osteoporosis Centers (UOC) Gainesville Georgia
United States Osteoporosis Clinical Trial Center Hagerstown Maryland
United States Northeast Clinical Research Hamden Connecticut
United States School of Medicine Indianapolis Indiana
United States Colorado Center for Bone Research Lakewood Colorado
United States University of Arkansas for Medical Science Little Rock Arkansas
United States Longmont Medical Research Network Longmont Colorado
United States Orthopaedic Hospital Los Angeles California
United States University of Tennessee Health Science Memphis Tennessee
United States West Cancer Clinic Memphis Tennessee
United States Arthritis Regional Research Center Mercerville New Jersey
United States Diabetes Regional Research Center Midland Texas
United States Winthrop U Hospital Mineola New York
United States Phoenix OB-GYN Associates, LLC Moorestown New Jersey
United States Medical Specialists Munster Indiana
United States Anchor Research Center Naples Florida
United States Health Core Newark Delaware
United States Hampton Roads Center for Clinical Research, Inc Norfolk Virginia
United States The Foundation for Osteoporosis Research and Education Oakland California
United States Arizona Arthritis Research Paradise Valley Arizona
United States Einstein Philadelphia Pennsylvania
United States Thomas Jefferson University Hospital Philadelphia Pennsylvania
United States University of Pittsburgh Pittsburgh Pennsylvania
United States Oregon Health and Science University Portland Oregon
United States Rhode Island Hospital, Osteoporosis Research/ Bone Density Unit Providence Rhode Island
United States Roger William Medical Center Providence Rhode Island
United States McGuire Veterans Affairs Medical Center Richmond Virginia
United States VA Commonwealth University Richmond Virginia
United States University of California Davis- Gen Med Research Sacramento California
United States Sam Clinical Research Center San Antonio Texas
United States Osteoporosis Prevention Center San Diego California
United States Radiant Research- San Diego San Diego California
United States Sarasota Arthritis Center Sarasota Florida
United States Osteoporosis Research Unit Seattle Washington
United States Avera Research Institute Sioux Falls South Dakota
United States The Physicians Clinic Spokane Washington
United States Washington University School of Medicine St. Louis Missouri
United States Radiant Stuart Florida
United States Southern Arizona VA Tucson Arizona
United States University of Texas Health Center at Tyler -Center for Clinical Research Tyler Texas
United States Diablo Clinical Research, Inc Walnut Creek California
United States Comprehensive Clinical Trials, LLC West Palm Beach Florida
United States Palm Beach Research Center West Palm Beach Florida
United States Heartland Research Associates, LLC Wichita Kansas
United States Clinical Pharmacology Study Groups Worcester Massachusetts
United States Radiant Wyomissing Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Novartis Pharmaceuticals

Countries where clinical trial is conducted

United States,  Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of hip fxs
Primary Incidence of new vertebral fxs
Secondary Percent change in hip BMD
Secondary New and/or worsening vertebral fxs
Secondary All clinical fxs
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