Dental Malocclusion and Craniofacial Development in OI

Status: Active_not_recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

Osteogenesis imperfecta (OI) is a rare inherited disorder that causes bones to break easily. Individuals with osteogenesis imperfecta break bones often and may have other problems, including hearing loss and pain and difficulty getting around. People with moderate to severe OI may also be diagnosed with dentinogenesis imperfecta (DI). DI is characterized by grey or brown teeth that may chip and wear down and break easily. People with DI may also have skull and neck defects. These patients may have severe teeth misalignment resulting in clinically significant chewing problems. Teeth misalignment in OI is very hard to treat because of the quality and quantity of bone. The overall goal of this study is to improve dental health to improve the quality of life of people with OI.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 10
Maximum Age: 100
Healthy Volunteers: f
View:

• Males and females with Clinical diagnosis of OI other than OI type I

• Individuals 10 years or older

• Participant of the Brittle Bone Disease (BBD) Longitudinal Study (7701)

Locations
United States
California
University of California Los Angeles
Los Angeles
Texas
Baylor College of Medicine
Houston
Other Locations
Canada
Shriners Hospital for Children
Montreal
Time Frame
Start Date: 2016-08
Completion Date: 2026-12
Participants
Target number of participants: 75
Sponsors
Collaborators: University of Nebraska, Children's National Research Institute, Hospital for Special Surgery, New York, Oregon Health and Science University, Hugo W. Moser Research Institute at Kennedy Krieger, Inc., Shriners Hospitals for Children, University of California, Los Angeles
Leads: Baylor College of Medicine

This content was sourced from clinicaltrials.gov