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Application of contralateral concentric circle method in preoperative planning for direct anterior approach total hip arthroplasty in the treatment of osteonecrosis of the femoral head

Application of concentric circle method in preoperative planning for direct anterior approach total hip arthroplasty in the treatment of osteonecrosis of the femoral head

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125243
Enrollment
Unknown
Registered
2026-05-22
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

Osteonecrosis of the femoral head

Interventions

Trial group (healthy-side concentric circle method digital preoperative planning group):Healthy-side concentric circle method digital preoperative planning (standard bilateral hip anteroposterior X-ra
the trial group additionally underwent three-dimensional CT reconstruction to assist in A-point identification
surgery performed by the same surgical team with >=5 years of experience in DAA-THA)
Control group (conventional template measurement method group):Conventional template measurement method (standard bilateral hip anteroposterior X-ray imaging before surgery

Sponsors

The People’s Hospital of Pizhou / Pizhou City Hospital, Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years, male or female; 2. Diagnosed with osteonecrosis of the femoral head (ONFH) according to the criteria of the Chinese "Clinical Diagnosis and Treatment Guidelines for Osteonecrosis of the Femoral Head," with etiologies including but not limited to corticosteroids, alcohol, trauma, etc.; 3. Failed conservative treatment, with significant pain and functional impairment, and meeting the indications for total hip arthroplasty (THA); 4. Normal hip joint function and no severe structural abnormalities on the non-operative side (healthy side); 5. Voluntary participation and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Pathological fracture or acute stage of femoral neck fracture; 2. Prior history of hip or femoral surgery on the ipsilateral lower limb; 3. Developmental dysplasia of the hip (DDH), severe osteoarthritis, or septic arthritis of the affected or healthy side hip joint; 4. Severe osteoporosis or metabolic bone disease (e.g., Paget's disease); 5. Multiple fractures or severe soft tissue injury of the lower limb; 6. Unable to tolerate surgery; 7. Psychiatric illness or inability to comply with follow-up visits.

Design outcomes

Primary

MeasureTime frame
COR Reconstruction Accuracy ;

Secondary

MeasureTime frame
Leg Length Discrepancy;Cup Abduction Angle and Anteversion Angle;Harris Hip Score;Forgotten Joint Score-12;Perioperative Complications;

Countries

China

Contacts

Public ContactDai Chengbai

The People’s Hospital of Pizhou / Pizhou City Hospital, Affiliated Hospital of Xuzhou Medical University

huangx0619@163.com+86 133 0832 7419

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026