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Functional Surgical Planning for Patients with Severe Sagittal Imbalance Undergoing Total Hip Arthroplasty: A Randomized Double-Blinded Control Study

Functional Surgical Planning for Patients with Severe Sagittal Imbalance Undergoing Total Hip Arthroplasty: A Randomized Double-Blinded Control Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120796
Enrollment
Unknown
Registered
2026-03-19
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Hip joint disorders requiring total hip arthroplasty

Interventions

Predicted PT Planning Group (Experimental Group):After hospital admission and provision of informed consent, standing and seated full-length anteroposterior-lateral radiographs obtained within 1 year
Preoperative PT Planning Group (Control Group):After hospital admission and provision of informed consent, standing and seated full-length anteroposterior-lateral radiographs obtained within 1 year pr

Sponsors

Beijing Jishuitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with severe spino-pelvic sagittal imbalance (SVA >=100mm) scheduled for unilateral total hip arthroplasty at the Department of Orthopaedic Surgery, Beijing Jishuitan Hospital.

Exclusion criteria

Exclusion criteria: 1. Patients scheduled for hip revision arthroplasty; 2. Patients undergoing THA due to pelvic fractures or active hip joint infections; 3. Patients planned for knee arthroplasty or spinal fusion surgery within 3 months postoperatively; 4. Patients with severe knee osteoarthritis; 5. Patients unable to stand preoperatively or with anticipated non-ambulatory status postoperatively; 6. Patients without sagittal balance restoration potential (e.g., prior lumbar fusion with fixed deformity); 7. Patients with SVA >150mm; 8. Patients with symptomatic contralateral hip osteoarthritis who decline or are ineligible for surgery.

Design outcomes

Primary

MeasureTime frame
Absolute error between the AI angle of the cup on the lateral radiograph and the preoperatively planned AI angle;

Secondary

MeasureTime frame
Proportion of AI angles falling outside the safe zone;Coronal plane angles of the acetabular cup: absolute differences between the standing radiographic inclination/anteversion angles and the preoperative plan;Parameters for postural change assessment: PT, SS, SVA, PI, LL, TK;Dislocation within 3 months postoperatively;Harris Hip Score (HHS) and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score.;Gender;Age;Height;Weight;Body Mass Index;Time of onset;

Countries

China

Contacts

Public ContactHao Tang

Beijing Jishuitan Hospital, Capital Medical University

pkuhao@163.com+86 136 9923 0055

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026