Pregnancy in Osteogenesis Imperfecta (OI) Registry
Completed
Conditions studied: Osteogenesis Imperfecta, Brittle Bone Disorders
In brief
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.
Key facts
- Study ID
- NCT03072303
- Run by
- University of South Florida
- People needed
- 170
- Starts
- 2017-06-16
- Expected to finish
- 2019-09-13
- Last updated by the study team
- 2019-10-16
Who can join
Age: any. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female with OI who has delivered an infant of at least 24 weeks' gestation
- Participant in the BBD Contact Registry
You may not qualify if…
- Inability to provide informed consent and complete survey
- Males
- Women with OI who have not delivered children and gestations associated with higher order multiples
Where it is running
- RDCRN Data Management and Coordinating Center, University of South Florida — Tampa, Florida, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.