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.
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
- Conditions the study is for
- Developmental Dysplasia of the Hip, Hip Dysplasia, Hip Dysplasia, Congenital
- 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.
Canada1 site, 1 recruiting
- Recruiting
BC Children's Hospital
Vancouver, British Columbia, V6H3N1
Emily Schaeffer, PhD, 604-875-2359, emily.schaeffer@cw.bc.ca
Kishore Mulpuri, FRCSC
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:
- Determine whether observation is non-inferior to bracing for infants with radiological dysplasia
- Provide a strong recommendation for management of this subset of DDH patients
- 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.
- Conditions
- Developmental Dysplasia of the Hip, Hip Dysplasia, Hip Dysplasia, Congenital, Hip Dysplasia, Developmental
- 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 group | Role | What they receive |
|---|---|---|
| Brace Treatment | Experimental | Patients randomized to the brace treatment group will be treated with a Pavlik harness for a minimum of six weeks. Receives: Other: Pavlik Harness |
| Active Monitoring | No intervention | Patients 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.
Acetabular Index
A measure of the steepness of the acetabular roof assessed on radiograph.
Measured: 2 years
Secondary outcomes (8)
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
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
Percent Femoral Head Coverage
Measured via ultrasound and assesses the percentage of the femoral epiphysis covered by the acetabular roof.
Measured: 6 weeks
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
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
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
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
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.
- First posted22 May 2023
- Study start25 Apr 2024
- Primary completionSep 2027 (estimated)
- Study completionSep 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Developmental Dysplasia of the HipStudies of the same condition, open and under way.
- More trials run by University of British ColumbiaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of British Columbia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Kishore Mulpuri, University of British Columbia
- Investigators
- Kishore Mulpuri, FRCSC, Principal investigator, University of British ColumbiaEmily Schaeffer, PhD, Study director, University of British Columbia
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
Study at a glance
From the registry record, last updated by the sponsor on 24 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of Brace to Observation in Stable, Radiological Developmental Dysplasia of the Hip: A Multi-centre, International Randomized Controlled Non-inferiority Trial
- ClinicalTrials.gov ID
- NCT05869851
- Acronym / sponsor ID
- H20-03750
- Conditions
- Developmental Dysplasia of the Hip, Hip Dysplasia, Hip Dysplasia, Congenital, Hip Dysplasia, Developmental
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 514 participants (estimated)
- Lead sponsor
- University of British ColumbiaUniversity, hospital or other
- Study start
- 25 Apr 2024 (actual)
- Primary completion
- Sep 2027 (estimated)
- Study completion
- Sep 2028 (estimated)
- First posted
- 22 May 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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:
- Determine whether observation is non-inferior to bracing for infants with radiological dysplasia
- Provide a strong recommendation for management of this subset of DDH patients
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Brace Treatment | Experimental | Other: Pavlik HarnessPatients randomized to the brace treatment group will be treated with a Pavlik harness for a minimum of six weeks. |
| Active Monitoring | No intervention | –Patients randomized to the control group will undergo observation only. |
Who may qualify
- Ages
- Up to 12 weeks
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (2 listed)
- 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
Key exclusion criteria (4 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Pavlik HarnessThe 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. | Other | Brace Treatment |
Primary outcome
Acetabular Index
Time frame: 2 years
A measure of the steepness of the acetabular roof assessed on radiograph.
8 secondary outcomes
Alpha Angle
Time frame: 6 weeks
Beta Angle
Time frame: 6 weeks
Percent Femoral Head Coverage
Time frame: 6 weeks
Number of Participants that Experienced Complications
Time frame: 2 years
Parent/Guardian Perception Questionnaire
Time frame: 6 weeks
EuroQoL-5D
Time frame: 6 weeks, 1 year, 2 years
Parent/Guardian Satisfaction
Time frame: 6 weeks, 1 year, 2 years
Healthcare Resource Use Questionnaire
Time frame: 6 weeks, 6 months, 1 year, 18 months, 2 years (Canadian centres only)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Nov 2025.
- Derived from this study: PubMed 38977361Zomar 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.
- Individual participant dataSharing planned: 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.
Related trials for Developmental Dysplasia of the Hip
Recruiting
SIRI Levels Following PENG Block in Pediatric Hip Surgery
Hip Dysplasia
RecruitingPhase 4
PENG With LFCB vs. ESP Blocks for Pediatric Hip Surgery
Hip Disease, Hip Dysplasia
Recruiting
EMPHASYS Cup Positioning in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN))
Osteoarthritis, Traumatic Arthritis
Not yet recruitingObservational study
3D-Printed Pelvic Models for Planning Complex Total Hip Arthroplasty
Developmental Dysplasia of the Hip, Acetabular Bone Loss
Active, not recruitingObservational study
The Medacta Quadra-P Anteverted Study
Arthrosis, Traumatic Arthritis
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Kishore Mulpuri, FRCSC principal investigator
University of British Columbia
Emily Schaeffer, PhD study director
University of British Columbia
1 site in 1 country: see every site and its status.
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.