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Parameters for Functional Mirror-Image Reconstruction in Total Hip Arthroplasty for Patients with Unilateral Developmental Dysplasia of the Hip

Parameters for Functional Mirror-Image Reconstruction in Total Hip Arthroplasty for Patients with Unilateral Developmental Dysplasia of the Hip

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129285
Enrollment
Unknown
Registered
2026-08-03
Start date
2026-08-10
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Developmental Dysplasia of the Hip

Interventions

Prospective Musculoskeletal Modeling Cohort:None
Retrospective Clinical Validation Cohort:None

Sponsors

Fourth Medical Center of the Chinese People's Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Part 1 (Prospective Modeling Study): 1. Preoperative diagnosis of unilateral Hartofilakidis type B or C DDH, with the other hip normal; 2. Have undergone primary THA for more than 1 year; 3. No serious postoperative complications such as prosthesis loosening, infection, or dislocation; 4. Complete CT imaging data available at the last postoperative follow-up; 5. Able to cooperate with gait analysis testing. Part 2 (Retrospective Validation Study): 1. Patients with unilateral Hartofilakidis type B/C DDH who had primary THA at our hospital; 2. Postoperative follow-up time >= 1 year; 3. Clear and measurable anteroposterior pelvic X-rays after surgery; 4. Able to cooperate with follow-up via phone or outpatient visits.

Exclusion criteria

Exclusion criteria: 1.Previous surgery on the affected hip; 2.Other serious hip disorders, such as infection or tumor; 3.Neuromuscular disorders that may substantially affect gait or lower-limb function; 4.Serious postoperative complications, including prosthetic loosening, infection, or recurrent dislocation; 5.Incomplete clinical records or inadequate-quality radiographic, CT, or gait-analysis data; 6.Inability to complete follow-up or refusal to permit the use of clinical data for this study.

Design outcomes

Primary

MeasureTime frame
Peak Gluteus Medius Muscle Force;Hip Joint Contact Force;Three-Dimensional Spatiotemporal Gait Parameter;Hip Joint Kinematic Parameters During Gait;Hip Joint Kinetic Parameters During Gait;Harris Hip Score;

Secondary

MeasureTime frame
Forgotten Joint Score-12;Gluteus Medius Muscle Volume;Gluteus Medius Attachment Area;Vertical Center of Rotation;Greater Trochanter Height;Acetabular Offset;Femoral Offset;Gluteus Medius Moment Arm;Gluteus Medius Moment-Arm Angle;Incidence of Postoperative Complications;

Countries

Chinese

Contacts

Public ContactChai Wei

Fourth Medical Center of the Chinese People's Liberation Army General Hospital

chaiwei301@163.com+86 136 0137 2998

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026