VicHip – Victorian hip dysplasia registry
- Project status: Active
Research area: Clinical Sciences > Orthopaedics
Our mission is to improve hip care and outcomes for patients with hip dysplasia through ground breaking research.
We are a group of families, hip health experts and researchers dedicated to learning more about hip dysplasia, its causes, and the most effective treatments.
We are a group of families, hip health experts and researchers dedicated to learning more about hip dysplasia, its causes, and the most effective treatments.
We are a group of families, hip health experts and researchers dedicated to learning more about hip dysplasia, its causes, and the most effective treatments.
Hip dysplasia
Hip dysplasia, also known as developmental dysplasia of the hip (DDH), is a common condition in children where the hip ball-and-socket joint doesn’t develop normally. Hip dysplasia can be mild or severe and affects one in every 100 babies.
If not treated, hip dysplasia can cause problems like pain and disability. It is also the underlying cause of one-quarter of hip replacements under the age of 50.
However, hip dysplasia is often easily treated when caught early. More key facts are available on the VicHip website.
VicHip
The Victorian hip dysplasia registry, or VicHip, is a clinical registry of patients diagnosed with hip dysplasia in Victoria.
A clinical registry collects and analyses confidential health information about people who have the same condition to help improve care and treatment for future patients. Through VicHip, we want to learn more about what causes hip dysplasia and how best to detect and treat it.
If your child has been diagnosed with hip dysplasia and sees a doctor at a participating hospital or clinic, we invite you to join VicHip. By sharing information about your child's health, you can help doctors establish a shared understanding of the screening and diagnostic evidence.
VicHip is run by Murdoch Children’s Research Institute (MCRI), with support from The Royal Children’s Hospital and the University of Melbourne and funded by the Australian Government Department of Health and Aged Care.
More information
Our research
VicHip registry data is used to understand hip dysplasia better, measure the quality of care provided and how it relates to patient outcomes.
Our research falls into three key focus areas:
- Cause and risks factors
- Early diagnosis and treatment
- Shaping a future of healthier hips
See the VicHip website for more information on our research focus areas.
Information for participants
VicHip is a group of families, researchers and doctors who are dedicated to sharing what they know about hip dysplasia.
Joining VicHip means you can actively participate in the development and ongoing improvement of the registry, its research and initiatives. Your experiences can help us improve hip care and outcomes for children and adults living with hip dysplasia.
If your child has been diagnosed with hip dysplasia and their doctor works at a participating hospital or clinic, a VicHip team member may contact you about joining the registry. Our team will explain what VicHip is and what’s involved, plus answer any questions you have.
If you choose to enrol in VicHip, we will follow your child's medical journey with hip dysplasia until they reach at least 16 years of age. For children undergoing surgery, we’d like to monitor their long-term health outcomes into adulthood. Your doctor or clinician will gather this anonymous data during your child's regular appointments, which will then be submitted to the registry for analysis.
Parents can find more out about the study at VicHip.
Information for health professionals
We work with hip specialists, orthopaedic surgeons, paediatricians, physiotherapists, orthotists, sonographers, midwives and nurses to enhance the quality of hip care and services throughout Victoria.
VicHip aims to provide clinicians with the tools and information needed to accurately diagnose and treat hip dysplasia.
We aim to create a shared understanding of how we screen and diagnose hip dysplasia, so we can treat and manage it more consistently. This could mean better care and results for people of all ages and could lower the chances of children developing long-term disability, painful osteoarthritis or the need for hip replacement.
Why join VicHip?
By working with us, you get to share your thoughts, suggest ways to make things better and talk about how health care for hip dysplasia should be.
Your input helps make sure doctors' opinions are heard when decisions are made.
Funding and collaborators
Thanks to our key partners, funders, and supporters.
Funding
- VicHip is funded by the Australian Government Department of Health and Aged Care under the Medical Research Future Fund grant.
Collaborations
- Barwon Health
- Monash Health
- Western Health
- Generation Victoria (GenV)
- British Columbia Children's Hospital Research Institute, Canada
- Global Hip Dysplasia Registry (GHDR), Canada
- International Hip Dysplasia Institute (IHDI), USA
- The Royal Children’s Hospital, Melbourne
- Victorian Orthopaedic Centre
Contact us
Victorian Hip Dysplasia Registry (VicHip)
Murdoch Children's Research Institute
The Royal Children's Hospital
50 Flemington Road
Parkville VIC 3052
Australia
Email: show email address