A Multicenter Study to Evaluate the Effects of DR-105 on Bone Mineral Density in Adolescent Females



Status:Archived
Conditions:Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:June 2009
End Date:March 2012

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Trial Summary
Trial Overview
Inclusion Criteria

A Multicenter, Open-Label, Randomized, Controlled Study to Compare the Effects on Bone Mineral Density of DR-105 and a 28-Day Cycle Oral Contraceptive Regimen in Healthy, Postmenarchal, Adolescent Females


This study is being conducted to compare the effects of DR-105 to a 28-day oral
contraceptive regimen on bone mineral density (BMD) in adolescent females. Subjects will be
randomized to either DR-105 or a 28-day oral contraceptive (OC). Subjects not seeking
hormonal contraception who meet eligibility criteria will serve as a control group. Duration
of the study for study subjects will be approximately 13 months.



We found this trial at
23
sites
Rhode Island Hospital
593 Eddy Street
Providence, Rhode Island 02903
401-444-4000
Rhode Island Hospital Founded in 1863, Rhode Island Hospital in Providence, RI, is a private,...
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Duramed Research Investigational Site
Baton Rouge, Louisiana 70808
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Baton Rouge, LA
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Duramed Research Investigational Site
Boynton Beach, Florida 33472
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Duramed Research Investigational Site
Champaign, Illinois 61820
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Champaign, IL
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Duramed Research Investigational Site
Cleveland, Ohio 44109
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Cleveland, OH
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Duramed Research Investigational Site
Columbia, South Carolina 29201
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Columbia, SC
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Methodist Charlton Cancer Ctr.
Dallas, Texas 75237
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Dallas, TX
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Duramed Research Investigational Site
Dallas, Texas 75237
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Duramed Research Investigational Site
Durham, North Carolina 27713
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Durham, NC
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Duramed Research Investigational Site
La Mesa, California 91942
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La Mesa, CA
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Teva Investigational Site
La Mesa, California 91942
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La Mesa, CA
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Duramed Research Investigational Site
Lawrence, New Jersey 08648
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Lawrence, NJ
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Duramed Research Investigational Site
Lincoln, Nebraska 68510
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Lincoln, NE
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Duramed Research Investigational Site
Little Rock, Arkansas 72204
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Little Rock, AR
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Duramed Research Investigational Site
Louisville, Kentucky 40202
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Louisville, KY
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Duramed Research Investigational Site
Medford, Oregon 97504
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Medford, OR
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Duramed Research Investigational Site
Norfolk, Virginia 23502
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Norfolk, VA
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Duramed Research Investigational Site
Pittsburgh, Pennsylvania 15213
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Pittsburgh, PA
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Teva Investigational Site
Port Jefferson, New York 11777
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Port Jefferson, NY
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Duramed Research Investigational Site
Salt Lake City, Utah 84107
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Salt Lake City, UT
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Duramed Research Investigational Site
Seattle, Washington 98105
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Seattle, WA
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Duramed Research Investigational Site
St. Louis, Missouri 63110
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Teva Investigational Site
Uniontown, Pennsylvania 15401
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