Effect of Teriparatide Compared to Risedronate on Back Pain in Women With a Spine Fracture Caused by Osteoporosis

PHASE3CompletedINTERVENTIONAL
Enrollment

712

Participants

Timeline

Start Date

June 30, 2006

Primary Completion Date

June 30, 2009

Study Completion Date

June 30, 2010

Conditions
Osteoporosis, PostmenopausalBack PainSpinal Fracture
Interventions
DRUG

teriparatide

20 ug/day, subcutaneous, 18 months

DRUG

risedronate

35 mg/once weekly, oral, 18 months

DRUG

placebo

once weekly, oral, 18 months

DRUG

placebo

daily, subcutaneous, 18 months

Trial Locations (72)

1180

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2031

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2217

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3000

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3145

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3300

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4000

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4558

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5035

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5530

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6534

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9000

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14000

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17176

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18012

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20354

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21120

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24047

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25801

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28046

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30033

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30501

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34684

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35033

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35294

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35619

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36111

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37000

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37007

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37067

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44195

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45000

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46017

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46202

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50322

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52525

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53100

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53705

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54449

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60053

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60528

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64461

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68131

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75185

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75679

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77054

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80084

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80335

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85381

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86000

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90185

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92653

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94609

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98144

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99204

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06030

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C1117ABH

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13073-350

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22271-100

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01246-903

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V6H 3X8

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R3A 1M3

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L8N 1Y2

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N6A 4V2

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H3A 1A1

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G1V 3M7

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G8Z 1Y2

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S7K 0H6

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D-69120

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04207

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00716

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00918

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All Listed Sponsors
lead

Eli Lilly and Company

INDUSTRY

NCT00343252 - Effect of Teriparatide Compared to Risedronate on Back Pain in Women With a Spine Fracture Caused by Osteoporosis | Biotech Hunter | Biotech Hunter