Global hip dysplasia registry for young children
Part of Bones, joints & muscles, Genetic & congenital, Injuries & trauma clinical trials.
This trial is a worldwide registry that collects information from children with hip dysplasia or who are at higher risk. It helps researchers understand who is affected and how hip evaluations are done, which can improve future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Be between 0 and 10 years old when you are first diagnosed
- Be referred for hip dysplasia screening because of risk factors or already diagnosed with hip dysplasia
- Have your hip diagnosis confirmed with a hip ultrasound or hip X-ray
- Have no known or suspected nerve/muscle, collagen, chromosome, or other lower-limb birth conditions
- Not have a hip dislocation related to a syndrome (a broader condition)
- Not have started hip dysplasia treatment already without proper imaging records or documentation
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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