Pregnancy in Osteogenesis Imperfecta (OI) Registry
NCT03072303 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 170
Last updated 2019-10-16
Summary
The purpose of this study is to learn about pregnancy outcomes in osteogenesis imperfecta (OI). Patients enrolled in the Brittle Bone Disorders (BBD) Contact Registry (CR) will be invited via email to participate in this study.
Conditions
- Osteogenesis Imperfecta
- Brittle Bone Disorders
Interventions
- OTHER
-
Web-based Survey
Patients will be sent an email invitation describing the study. If the participant wants to participate and is eligible, she will follow the survey link in the email message, which directs her to an IRB-approved online consent form. A unique survey link will be generated for each participant and included in the survey invitation, which is a customized email message. This link will allow the investigators to determine who completed the survey. The investigators will send repeat email invitations every two months (total of 3 invitations) to those invitees who have not yet participated. The investigators will allow approximately 6 months for enrollment and survey completion and expect that the study will close soon thereafter.
Sponsors & Collaborators
-
Rare Diseases Clinical Research Network
collaborator NETWORK -
National Institutes of Health (NIH)
collaborator NIH -
University of South Florida
lead OTHER
Principal Investigators
-
Jeffrey Krischer, Ph.D. · University of South Florida
-
Deborah Krakow, M.D. · University of California, Los Angeles
Eligibility
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-06-16
- Primary Completion
- 2019-03-13
- Completion
- 2019-09-13
Countries
- United States
Study Locations
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