CompletedNot Applicable

Pregnancy in Osteogenesis Imperfecta (OI) Registry

United States170 participantsStarted 2017-06-16

Plain-language 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.

Who can participate

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Female with OI who has delivered an infant of at least 24 weeks' gestation * Participant in the BBD Contact Registry Exclusion Criteria: * Inability to provide informed consent and complete survey * Males * Women with OI who have not delivered children and gestations associated with higher order multiples

What they're measuring

Pregnancy in OI Assessment

Timeframe: 1 year

Trial details

NCT IDNCT03072303

SponsorUniversity of South Florida

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2019-03-13

View on ClinicalTrials.gov More Osteogenesis Imperfecta trials