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Development of Intelligent Diagnosis Technology for Operative and Endodontic Diseases

Development of Intelligent Diagnosis Technology for Operative and Endodontic Diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109129
Enrollment
Unknown
Registered
2025-09-12
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Dental caries, Pulpitis, Periapical periodontitis

Interventions

Intelligent Diagnosis Group:Artificial intelligence is used to analyze CBCT data.
Traditional diagnosis group:Manual analysis of CBCT data

Sponsors

West China Hospital of Stomatology,Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Task 1 & 3: 1. Images must be clear and free of artifacts that severely impact diagnosis and algorithm performance. 2. The scan range must completely encompass the target tooth/teeth, extending from the crown to at least 3mm beyond the root apex to ensure the entire root and apical foramen are included. 3. The field of view must cover three teeth. 4. Target areas must include anterior teeth, premolars, and molars. Task 2: 1. Images must be clear and free of artifacts that severely impact diagnosis. 2. The scan range must completely include the crown and cervical region of the target tooth and at least one adjacent tooth (except in free-end situations). 3. Target areas must include anterior teeth, premolars, and molars. 4. For proximal caries (mesial and distal), bitewing radiographs or images acquired using the parallel technique are required for caries classification. Task 4: This task will utilize previously collected extracted teeth and does not require patient involvement.

Exclusion criteria

Exclusion criteria: Task 1: 1. Root canal retreatment cases with root canal filling material extruding beyond the apical foramen. 2. Severe artifacts that obscure or prevent identification of key measurement landmarks (e.g., pulp chamber walls, root canal walls, apical foramen). 3. Conditions preventing clinical root canal length measurement, such as a large apical foramen, external root resorption, root fracture, lateral perforation, or root crack. 4. Severe coronal destruction where normal anatomical contours cannot be defined, preventing determination of a coronal reference point. 5. Excessive scanning slice thickness that cannot meet the precision requirements for fine measurements. Task 2: 1. Severe artifacts that prevent clear delineation of enamel, dentin, carious areas, restoration margins, or pulp chamber boundaries. 2. Extensive coronal defects that preclude effective assessment of caries extent. 3. Excessive scanning slice thickness that cannot meet the diagnostic requirements for detecting minute carious lesions. Task 3: 1. Artifacts or scanning parameters (e.g., slice thickness) that cannot meet the precision requirements for fine measurements. Task 4: This task will utilize previously collected extracted teeth and does not require patient involvement.

Design outcomes

Primary

MeasureTime frame
Root canal length;Caries types;Root Canal Treatment Difficulty Classification;Quantify structural differences between CBCT and uCT;

Countries

China

Contacts

Public ContactChenglin Wang

West China Hospital of Stomatology,Sichuan University

wxonet@163.com+86 134 0840 1978

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026