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A multicenter, prospective, randomized, 2-way crossover, open-label study in postmenopausal women with osteoporosis examining subject satisfaction and compliance when risedronate sodium [risedronic acid](Actonel) is administered 35mg once a week or 5mg once daily.

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Trial Profile

A multicenter, prospective, randomized, 2-way crossover, open-label study in postmenopausal women with osteoporosis examining subject satisfaction and compliance when risedronate sodium [risedronic acid](Actonel) is administered 35mg once a week or 5mg once daily.

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 16 Jul 2009

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At a glance

  • Drugs Risedronic acid (Primary)
  • Indications Postmenopausal osteoporosis
  • Focus Therapeutic Use
  • Sponsors Sanofi

    • Most Recent Events

    • 07 Jun 2007 New trial record.

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