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Enrolling by invitationNCT07066852Updated Sep 18, 2025

Evaluation of the Effectiveness of Developmental Hip Dysplasia Screening in Risk Groups

An observational study in Developmental Dysplasia of Hip, sponsored by Ankara City Hospital Bilkent. Enrolling by invitation at 1 site in Turkey (Türkiye). Per ClinicalTrials.gov, last updated 2025-09-18.

Sponsored by Ankara City Hospital Bilkent · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
300
Sex
All
01

Study summary

This study is a non-drug clinical trial.

Developmental dysplasia of the hip (DDH) encompasses a spectrum of hip developmental disorders, including dislocation, subluxation, and acetabular dysplasia. DDH is among the most prevalent hip conditions in infants. Dislocation is defined as the incomplete displacement of the hip joint, and residual dislocation due to DDH is associated with pain and severe osteoarthritis of the hip in young adulthood.

The progression of DDH is dynamic and may improve or worsen depending on various factors. The primary determinant of prognosis is the concentric reduction of the hip joint, with the femoral head needing to be reduced to allow for normal acetabular development.

DDH is the most common orthopedic condition in the neonatal period. According to the literature, the incidence is approximately 1:100 for dysplasia and 1:1000 for dislocation. However, estimates suggest that dislocation rates in Türkiye may reach 5-15:1000. DDH occurs six times more frequently in girls than boys and is more commonly observed in the left hip. Established risk factors for DDH include being a first-born girl, Caucasian race, positive family history, oligohydramnios, multiple pregnancies, in utero breech presentation, pes calcaneovalgus, metatarsus adductus, and torticollis.

Early detection and treatment of dislocation caused by DDH are associated with success rates exceeding 80%. However, diagnosis and treatment initiation after one year of age often result in variable outcomes. Literature indicates that clinical and sonographic evaluations may be normal at six weeks in breech patients-who are at significant risk for DDH-yet hip dysplasia may still develop in this population later. The investigators aim to contribute to existing literature by evaluating whether sonographic screening alone is sufficient or if additional screening methods are warranted for patients with identified DDH risk factors.

Read the detailed description

Study Overview This study aims to evaluate the effectiveness of developmental dysplasia of the hip (DDH) screening in high-risk pediatric groups in Türkiye.

In Türkiye, all newborns undergo routine hip ultrasonography during the second month of life. If the results are normal, no further hip evaluations are typically performed. However, incidental detection of acetabular dysplasia in children-who later undergo pelvic anteroposterior (AP) X-rays for unrelated reasons-has raised concerns regarding the sufficiency of current screening protocols. Recent studies emphasize that hip development is a dynamic process, with the first 18 months being critical for early intervention. The timely detection of hip dysplasia is essential to minimize long-term physical and psychological burden on patients and healthcare systems. Undiagnosed cases often result in the need for total hip replacement surgery in adulthood. Accordingly, there is a need for a large-scale, prospective study to broaden and enhance the scope of DDH screening, both nationally and globally.

Study Population and Screening Protocol Participants will include all children born in the high-risk pregnancy ward at Ankara Bilkent City Hospital, selected via randomized sampling. After obtaining informed consent from families, hip ultrasonography will be performed six weeks postpartum using the Graf classification method. The screening will include Ortolani-Barlow maneuvers, Galeazzi sign assessment, swaddling practices, and evaluation of associated foot deformities. All sonographic assessments will be conducted by a single, qualified physician.

In cases where pathology is detected, treatment will be initiated in accordance with current medical guidelines. The Graf-based ultrasonography will be repeated at the third month, and follow-up clinical notes will be documented. At six months of age, pelvic AP and frog-leg lateral X-rays will be obtained. The acetabular index will be assessed using the Tönnis grading system, and any limitations in abduction will be recorded. At one year of age, follow-up X-rays will be performed to reassess the acetabular index and Tönnis grade, facilitating longitudinal monitoring of hip development during infancy.

Ethics and Statistical Evaluation Ethics approval for this study was granted by the Ethics Committee of Ankara Bilkent City Hospital (Board No. 1). Power analysis indicated a required sample size of 185 participants to achieve a statistical power of 0.95. This study will be conducted prospectively and analyzed using SPSS version 26.0. Findings will be reported to the Ministry of Health of Türkiye upon study completion.

02

Conditions studied

  • Developmental Dysplasia of Hip

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Keywords

  • acetabulardysplasia
  • screening
  • ultrasound
  • xray
  • developmentaldysplasiaofhip
  • PediatricOrthopedics
03

In context

Hip Dislocation

107 studies on the registry are indexed under Hip Dislocation; 36 are open to participants now.

This study's planned enrollment of 300 is above the median of 120 across 39 observational studies indexed under Hip Dislocation.

Browse Hip Dislocation studies →

Lead sponsor

Ankara City Hospital Bilkent is the lead sponsor of 443 studies on the registry; 111 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

The study will include all children born in the high-risk pregnancy service at our hospital. Participants will be selected randomly, and their families will be informed about the study, providing consent for participation. The study aims to evaluate the effectiveness of developmental hip dysplasia (DDH) screening in high-risk groups in Turkey. Hip ultrasound will be performed six weeks after birth using the Graf method for screening purposes. This examination will include the Ortolani-Barlow test, Galeazzi sign, swaddling, and assessment of any accompanying foot deformities. All ultrasounds will be conducted by a single physician. If any pathology is detected, treatment will be initiated according to current literature. Follow-up evaluations will be conducted at three months, six months, and one year to monitor hip development and assess the acetabular index using Tönnis grading and abduction limitation.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All girls and boys of Turkish origin born in our hospital were included in our study.

Exclusion criteria

Exclusion Criteria:

  • Teratological hip diseases with neuromuscular disorders were excluded from our study. Parents who disrupted follow-up were excluded from the study.
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
300 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • sample

    we use one arm and one sample

    Radiation: x ray · Diagnostic Test: ultrasound

Interventions

  • Radiationx ray

    we performed pelvis ap and frog leg x ray to child in 6 month and 1 age

  • Diagnostic testultrasound

    we will perform ultrasound in 6 week and 3 month

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What researchers measure

Primary outcomes

  1. Acetabular Index Variation Measured by Tönnis Grading System

    The change in acetabular index will be assessed using pelvic anteroposterior(AP) and frog-leg lateral x-rays. Measurements will be analyzed according to the classification system. The unit of measure will be degrees(°).

    Time frame: At 6 months and 1 year of age

Secondary outcomes

  1. Incidence of Pathological Findings on Graf Ultrasonography

    Rate of infants showing sonographic abnormalities(types 2b,2c,d,3,4) on graf uulrasound.Assessment will indclude morphological classification using Graf's criteria.Unit of measure:% of screened participants.

    Time frame: At 6 weeks and 3 months after birth

07

Study locations

1 site
  • Department of Orthopedics and Traumatology, Bilkent City Hospital, Ankara
    Ankara, Ankara 06340, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: Yes — I plan to share the code with famous journals as proof that I have done a prospective study. In addition, since this study means 1-year hip follow-up of 340 children and there is no follow-up of this size, I want it for proof purposes

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report, Analytic code

Time frame: october 2024-october 2034

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2024 (actual). Primary completion is estimated for Dec 2025, 23 months after the start.

Of 20 observational studies under Hip Dislocation, half reached primary completion within 83 months of starting (the median), counting those still running; a quarter within 41 and three quarters within 113. This study's planned 23 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 12, 2024
First posted
Jul 15, 2025
StartActual
Jan 1, 2024
Primary completionEst.
Dec 31, 2025
CompletionEst.
Nov 1, 2026
Last update
Sep 18, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07066852
Responsible party
KENAN ŞEN (Principal Investigator, Orthopedics and Traumatology Assistant, Ankara City Hospital Bilkent) — Principal investigator
First posted
Jul 15, 2025
Start date
Jan 1, 2024
Primary completion
Dec 31, 2025 (estimated)
Completion
Nov 1, 2026 (estimated)
Last update
Sep 18, 2025

Study contacts

Mehmet Safa Kapıcıoğlu, Proffesor
study director · Department of Orthopedics and Traumatology, Bilkent City Hospital, Ankara
Mehmet Safa Kapıcıoğlu, Proffesor
principal investigator · Department of Orthopedics and Traumatology, Bilkent City Hospital, Ankara

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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