Clinical Trials Directory

Trials / Completed

CompletedNCT00159419

Bisphosphonate Therapy for Osteogenesis Imperfecta

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Indiana University School of Medicine · Academic / Other
Sex
All
Age
3 Years – 21 Years
Healthy volunteers
Not accepted

Summary

The study is designed to evaluate the efficacy and safety of "Bisphosphonate Therapy for Osteogenesis Imperfecta (OI)." We, the researchers at Indiana University School of Medicine, are characterizing the changes effected by oral bisphosphonate therapy and comparing them to a regimen of intravenous bisphosphonate therapy in a group of children with OI and also in children with other disorders that result in low bone mass and fractures.

Detailed description

The study is designed to evaluate the efficacy and safety of "Bisphosphonate Therapy for Osteogenesis Imperfecta (OI)." OI is an inherited disorder of collagen synthesis. Collagen is the major structural protein of the matrix of tendons, skin, and bones. Affected persons have low bone mineral density (and experience multiple fractures and progressive bony deformity). In its most severe form, the disorder is lethal in infancy. We plan to characterize the changes effected by oral bisphosphonate therapy and compare them to a regimen of intravenous bisphosphonate therapy in a group of children with OI. Additionally, we have begun to treat patients with OI and other conditions of low bone mineralization for age who are not eligible for the standard protocol (too young, history of abdominal pain, etc.) with bisphosphonate. We also plan to screen the parents and siblings of our patients diagnosed with osteogenesis imperfecta, in order to determine if they also have osteoporosis.

Conditions

Interventions

TypeNameDescription
DRUGAlendronate
DRUGPamidronate

Timeline

Start date
1999-08-01
Primary completion
2008-08-01
Completion
2008-08-01
First posted
2005-09-12
Last updated
2017-06-14
Results posted
2016-03-31

Source: ClinicalTrials.gov record NCT00159419. Inclusion in this directory is not an endorsement.