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Developmental Dysplasia of the HipNCT05869851

Developmental Dysplasia of the Hip: Observation vs. Bracing

A study testing Pavlik Harness in people with Developmental Dysplasia of the Hip and Hip Dysplasia, run by University of British Columbia at 1 site in Canada.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Developmental dysplasia of the hip (DDH) is the most common childhood hip condition. When caught early, bracing is the most frequently used treatment; however, the brace can disrupt important mother-baby bonding time in the newborn period and present challenges to daily living. Read more about this study

Who is it for?
Ages Up to 12 weeks
What is being tested?
Pavlik Harness
Could I receive a placebo?
No, everyone receives an active treatment
How many people
514 participants
Where
1 siteCanada
Study dates
25 Apr 2024to Sep 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 12 weeks
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Patients presenting with radiological dysplasia of a clinically stable hip under three months (12 weeks) of age
  • Radiological dysplasia will be defined as a centred hip with an alpha angle between 43 and 60 degrees and a percent coverage of the femoral head (FHC) greater than 35%, as measured on ultrasound exam

Who cannot join

  • Patients presenting with radiological dysplasia older than three months (12 weeks) of age
  • Patients presenting with clinical hip instability (Ortolani or Barlow positive)
  • Patients with known or suspected neuromuscular, collagen, chromosomal or lower-extremity congenital abnormalities or syndromic-associated hip abnormalities
  • Patients who received prior treatment (i.e. Pavlik harness) for DDH

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Emily Schaeffer, PhD contact

604-875-2359

emily.schaeffer@cw.bc.ca

Bryn Zomar, PhD contact

604-875-2359

bryn.zomar@cw.bc.ca

Canada1 site, 1 recruiting
  • BC Children's Hospital

    Vancouver, British Columbia, V6H3N1

    Emily Schaeffer, PhD, 604-875-2359, emily.schaeffer@cw.bc.ca

    Kishore Mulpuri, FRCSC

    Recruiting

Other trials in Canada

About this study

Official title: Comparison of Brace to Observation in Stable, Radiological Developmental Dysplasia of the Hip: A Multi-centre, International Randomized Controlled Non-inferiority Trial

Developmental dysplasia of the hip (DDH) is the most common childhood hip condition. When caught early, bracing is the most frequently used treatment; however, the brace can disrupt important mother-baby bonding time in the newborn period and present challenges to daily living. In babies with mild DDH, some studies have suggested that their hips may improve naturally as they grow and develop. This study will look at whether careful monitoring can be just as good as bracing for babies diagnosed with mild DDH less than 3 months of age, potentially avoiding unnecessary treatment. This will be the first study to look at this question with babies being treated at different hospitals in seven different countries, so the results will make an impact on children and families worldwide.

Read the detailed description

Early detection of developmental dysplasia of the hip (DDH) is critical to optimize outcomes and minimize long-term disability and impact on quality of life for the child and family. The burden of disease is significant, with a DDH diagnosis in 15-20/1000 live births. Even when treated, DDH is a leading cause of early hip replacement or development of osteoarthritis in young adults, with DDH reportedly accounting for 10-92% of all hip replacements. Consideration must also be given, however, to potential overtreatment of infants, particularly in more mild cases of hip instability or radiological dysplasia. The hip joint is immature during infancy, and many cases of mild-to-moderate DDH can spontaneously resolve as the hip joint matures through development. Brace treatment for approximately six weeks is common to address this radiological dysplasia; however, it is unclear whether this approach provides significant benefit above careful observation by ultrasound. While a conservative, less costly approach, brace treatment is not without potential complications and drawbacks. There are still substantial healthcare costs and resources associated with brace treatment, but there is potentially an under-recognized psychosocial cost in regard to preventing or disrupting mother-infant bonding in the newborn period. Coping with the difficulties of brace treatment can be stressful for families, particularly mothers of newborns, but the ultimate psychosocial impact has been under-researched to date. There is evidence to suggest that events occurring during establishment of breastfeeding may impact the mother's ability to breastfeed. The UK Hip Trial (2005) also found that maternal anxiety and worries about their infant's hip were increased with early brace treatment, but were not elevated by ultrasound monitoring in isolation. Further, bracing can present challenges to daily family life, including dressing, mobility, and the need for specialized furniture, car seats and other equipment. If observation alone is non-inferior to bracing for radiological dysplasia, unnecessary treatment may be avoided, potentially decreasing both the psychosocial impact of disrupted mother-infant bonding and needed healthcare resources and costs.

The investigators propose to utilize the existing collaborations and infrastructure of the Global Hip Dysplasia Registry (GHDR) and leverage their collaboration with a group in the Netherlands performing a similar Treatment with Active Monitoring (TRAM) trial to determine whether observation alone is sufficient for infants with clinically stable radiologically abnormal hips. Specifically, the investigators aim to:

  1. Determine whether observation is non-inferior to bracing for infants with radiological dysplasia
  2. Provide a strong recommendation for management of this subset of DDH patients
  3. Compare findings to those of the Netherlands trial, which is being carried out in older patients (10-16 weeks at diagnosis)

This study will utilize the established infrastructure of the GHDR. GHDR was established in 2016, aimed at collecting longitudinal data on infants and children across the entire DDH spectrum. This specific trial will function as a targeted sub-study within the more extensive registry, and is a multi-centre, international prospective randomized non-inferiority trial designed to evaluate the necessity to treat infants with radiological hip dysplasia. In total, 14 of the centres currently contributing data to GHDR have agreed to participate and randomize eligible patients.

Being tested
Pavlik Harness
Medical subject headings
Developmental Dysplasia of the Hip, Hip Dislocation, Hip Dislocation, Congenital

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pavlik HarnessOther

    The Pavlik harness is an abduction brace used for treatment of hip dysplasia in infants. It keeps the hips in proper alignment to allow for appropriate growth and development of the joint.

Study groups in NCT05869851
Study groupRoleWhat they receive
Brace TreatmentExperimentalPatients randomized to the brace treatment group will be treated with a Pavlik harness for a minimum of six weeks.
Receives: Other: Pavlik Harness
Active MonitoringNo interventionPatients randomized to the control group will undergo observation only.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Acetabular Index

    A measure of the steepness of the acetabular roof assessed on radiograph.

    Measured: 2 years

Secondary outcomes (8)
  1. Alpha Angle

    This angle is measured via ultrasound and refers to the angle between the acetabular roof and vertical cortex of the ilium.

    Measured: 6 weeks

  2. Beta Angle

    This angle is measured via ultrasound and refers to the angle formed between the vertical cortex of the ilium and the triangular labral fibrocartilage (echogenic triangle).

    Measured: 6 weeks

  3. Percent Femoral Head Coverage

    Measured via ultrasound and assesses the percentage of the femoral epiphysis covered by the acetabular roof.

    Measured: 6 weeks

  4. Number of Participants that Experienced Complications

    Including development of femoral nerve palsy or avascular necrosis, progression of hip dysplasia, and need for further treatment.

    Measured: 2 years

  5. Parent/Guardian Perception Questionnaire

    A survey assessing parent/guardian perceptions of caring for and bonding with their child. Each question is scored on a 7-point likert scale from 3 (strongly agree) to -3 (strongly disagree) with total scores ranging from 33 to -33.

    Measured: 6 weeks

  6. EuroQoL-5D

    A survey assessing parent quality of life. Only the VAS portion of the questionnaire will be asked at each visit. The VAS is scored from 0 to 100 with higher scores indicating better health.

    Measured: 6 weeks, 1 year, 2 years

  7. Parent/Guardian Satisfaction

    Assessed using a VAS scored from 0 to 100 with higher scores indicating higher satisfaction.

    Measured: 6 weeks, 1 year, 2 years

  8. Healthcare Resource Use Questionnaire

    Parent/guardian reported questionnaire to collect information about visits to health care professionals, imaging, medication use, additional treatments related to the diagnosis of DDH, and out of pocket costs.

    Measured: 6 weeks, 6 months, 1 year, 18 months, 2 years (Canadian centres only)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 May 2023
  2. Study start25 Apr 2024
  3. Primary completionSep 2027 (estimated)
  4. Study completionSep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
514 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05869851
Sponsor's protocol ID
H20-03750
Status last verified
Nov 2025
First submitted
10 May 2023
Last updated
24 Nov 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: While we will not make individual participant data available for this study, we do intend to disseminate study results to participants, researchers and the broader public. Our team works closely with patient partners, healthcare personnel, our collaborators and the broader medical/scientific community to determine appropriate ways to disseminate study results. We intend to prepare plain language summaries and visual/video abstracts of study results, which will be emailed to participants (those whom provided consent for email contact). These visual abstracts will also be posted to our lab's social media accounts, as well as that of our supporter, the I'm a HIPpy Foundation, who works closely with our patient and family community.

Publications

  • Zomar BO, Bone JN, Nguyen V, Mulpuri K, Kelley S; GHD Study Group; Schaeffer EK. Comparison of brace to observation in stable, radiological developmental dysplasia of the hip: a protocol for a global multicentre non-inferiority randomised trial. BMJ Open. 2024 Jul 8;14(7):e084738. doi: 10.1136/bmjopen-2024-084738.

    PubMed 38977361

Questions about this trial

What is this clinical trial studying?

A study testing Pavlik Harness in people with Developmental Dysplasia of the Hip and Hip Dysplasia, run by University of British Columbia at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 24 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Emily Schaeffer, PhD (604-875-2359, emily.schaeffer@cw.bc.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Acetabular Index (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05869851, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Nov 2025.

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