Actively Recruiting

Phase Not Applicable
Age: 4Weeks - 20Weeks
All Genders
Healthy Volunteers
NCT06647225

Using Artificial Intelligence to Screen for Hip Dysplasia

Led by Murdoch Childrens Research Institute · Updated on 2026-04-08

240

Participants Needed

1

Research Sites

99 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if an ultrasound scan using artificial intelligence can accurately screen for hip dysplasia. Researchers will compare the artificial intelligence ultrasound results to the standard ultrasound measures to see if the artificial intelligence ultrasound scan can accurately screen for hip dysplasia. It will also seek to understand how parents feel about their children undergoing this scan. Participants will: * Have an additional ultrasound performed on their child at their scheduled outpatient's appointment for hip dysplasia * Complete a short questionnaire about the experience of having the measurement performed on their child

CONDITIONS

Official Title

Using Artificial Intelligence to Screen for Hip Dysplasia

Who Can Participate

Age: 4Weeks - 20Weeks
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Enrolled in the VicHip study
  • Aged between 4 and 20 weeks at enrollment
  • Attending The Royal Children's Hospital for possible DDH diagnosis
  • Receiving a standard diagnostic hip ultrasound on the day of their outpatient appointment
  • Has a legally acceptable representative able to understand and provide informed consent
Not Eligible

You will not qualify if you...

  • Currently receiving treatment for Developmental Dysplasia of the Hip (DDH)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Royal Children's Hospital

Parkville, Victoria, Australia, 3052

Actively Recruiting

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Research Team

N

Natalie K Hyde, BBiomedSc (Hons), PhD

CONTACT

M

Melissa Formosa

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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