Pregnancy in Osteogenesis Imperfecta (OI) Registry
Status: Recruiting Summer 2017
What is the purpose of this study?
The purpose of this study is to learn about pregnancy outcomes in women with Osteogenesis Imperfecta (OI).
What does this study involve?
This is a self-report survey that will review pregnancy outcomes (maternal and fetal). Measures of pregnancy outcome will include 1) length of gestation, 2) mode of delivery, 3) neonatal outcomes including birth weight and length, 4) history of back pain or hip pain and or fractures during pregnancy or postpartum 5) number of maternal hospital admissions 6) calcium and vitamin D intake, 7) neonatal complications and 8) OI status in the fetus. This survey will take approximately 20 minutes to complete. One survey will be completed for each gestation (pregnancy).
The information collected for this study will be stored in a computer database at the Data Management and Coordinating Center at the University of South Florida in Tampa, FLof the Rare Diseases Clinical Research Network (RDCRN) and also sent to a Federal data repository (dbGaP). A data repository provides a way for researchers to store the information collected during the research study for future research studies. The data management center uses several layers of protection for the clinical data stored in its computer database. It meets all of the local and federal security requirements for research datacenters.
How many people will be in this study?
To be able to participate, you must be:
- A woman with OI who has delivered children
- Registered in the RDCRN Brittle Bone Disorders Consortium (BBD) Contact Registry
What are the possible risks of the study?
The only risk of participation is the potential loss of privacy, similar to that encountered through everyday use of the internet.
Are there benefits to being in the study?
There are no direct benefits to you for completing the survey. By taking part in this survey you may contribute to knowledge and future research of brittle bone disorders.
Will taking part in this research study cost me anything?
There are no costs to you for participating in this research study.
Registration on ClinicalTrials.gov
A description of this clinical trial will be available on http://www.ClinicalTrials.gov. This website will not include information that can identify you. At most, the website will include a description of the study or a summary of the results. You can search this website at any time.
Who do I contact for questions?
We greatly appreciate your interest in this study and in advancing the understanding of Osteogenesis Imperfecta.
In order to participate, you must personally contact the study project manager by phone or by e-mail. Please use the information below to inquire about participation.
Principal Investigator: Deborah Krakow, M.D.
University of California Los Angeles
Contact: Amoy Fraser, Study Project Manager
Address: University of South Florida
3650 Spectrum Blvd, Suite 100,
Tampa, Florida 33612-9446