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Construction and research of artificial intelligence digital diagnosis and operation design system for jaw malformation

Construction and research of artificial intelligence digital diagnosis and operation design system for jaw malformation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127071
Enrollment
Unknown
Registered
2026-06-24
Start date
2022-04-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Dentofacial deformities

Interventions

Intelligent Group:None
Human group:None

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient has a clear preoperative diagnosis of dentofacial deformity and needs orthognathic surgery; 2. Underwent digital surgical planning and splint fabrication; 3. Has preoperative digital dental models and final occlusion records; 4. Only underwent LeFort I osteotomy of the maxilla and bilateral sagittal split osteotomy of the mandible during surgery, with or without genioplasty; 5. Only involves clinically common types of dentofacial deformities.

Exclusion criteria

Exclusion criteria: 1. The patient needs to undergo apicoectomy based on their preoperative diagnosis; 2. The patient has systemic diseases, a history of trauma, jaw osteomyelitis, or has been diagnosed with cleft lip and palate, hemifacial microsomia, or other craniofacial syndromes; 3. The patient withdraws from the study for other reasons or cannot complete postoperative follow-up.

Design outcomes

Primary

MeasureTime frame
The difference between intelligent solutions and traditional surgical digitization, including the amount of maxillary advancement or retraction, maxillary gap or bone removal, error in dental and bony;

Secondary

MeasureTime frame
Based on the anesthesia records and surgical records of each subject, the operation time, blood loss, and intraoperative bone adjustment conditions of the two groups were evaluated. The surgical safet;Patient satisfaction with the overall surgical outcome at T0 and T3 stages;

Countries

China

Contacts

Public ContactEn Luo

West China Hospital of Stomatology, Sichuan University

79310781@qq.com+86 28 8550 3530

Outcome results

None listed

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