CompletedPhase 3NCT00106028
Safety and Efficacy of Risedronate in the Treatment of Osteogenesis Imperfecta in Children
Studying Osteogenesis imperfecta
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Warner Chilcott
- Principal Investigator
- Dietrich H Wenderoth, MD, MDProcter and Gamble
- Intervention
- risedronate sodium (Actonel)(drug)
- Enrollment
- 143 enrolled
- Eligibility
- 4-15 years · All sexes
- Timeline
- 2004 – 2010
Study locations (20)
- Miami Children's Hospital, Miami, Florida, United States
- University of Nebraska Medical Center, Children's Hospital, Omaha, Nebraska, United States
- Hospital for Special Surgery, New York, New York, United States
- Wright State University BioMedical Imaging Laboratory and Miami Valley Hospital, Dayton, Ohio, United States
- Oregon Health & Science University, Portland, Oregon, United States
- The Children's Hospital at Westmead, Westmead, New South Wales, Australia
- Princess Margaret Hospital for Children, Perth, Australia
- Cliniques Universitaires Saint Luc, Brussels, Belgium
- Pontificia Universidad Catolica de Chile, Santiago, Chile
- Osteocentrum, II. Interní klinika, Fakultní nemocnice Plzeň-Bory, Pilsen, Czechia
- Hospital for Children and Adolescents, Helsinki, Finland
- Klinikum und Poliklinik für Kinderheilkunde der Universität zu Köln, Cologne, Germany
- 2nd Department of Pediatrics, Semmelwies University, Faculty of Medicine, Budapest, Hungary
- Rheumatologic Rehabilitation Unit of the University of Verona, Valeggio sul Mincio, Italy
- Zaklad Biochemii i Medycyny Doswiadczalnej (Biochemisty Dept, Institute "Monument-Children Health Centre", Warzawa-Międzylesie, Poland
- +5 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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