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Development of Three-dimensional Deep Learning for Automatic Design of Skull Implants

Development of Three-dimensional Deep Learning for Automatic Design of Skull Implants

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05603949
Enrollment
6
Registered
2022-11-03
Start date
2023-02-03
Completion date
2023-07-15
Last updated
2023-02-13

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

Conditions

Skull Defect

Keywords

Deep Neural Networks;3D Shape Inpainting

Brief summary

This project aims to develop an effective deep learning system to generate numerical implant geometry based on 3D defective skull models from CT scans. This technique is beneficial for the design of implants to repair skull defects above the Frankfort horizontal plane.

Detailed description

Designing a personalized implant to restore the protective and aesthetic functions of the patient's skull is challenging. The skull defects may be caused by trauma, congenital malformation, infection, and iatrogenic treatments such as decompressive craniectomy, plastic surgery, and tumor resection. The project aims to develop a deep learning system with 3D shape reconstruction capabilities. The system will meet the requirement of designing high-resolution 3D implant numerical models efficiently. A collection of skull images were used for training the deep learning system. Defective models in the datasets were created by numerically masking areas of intact 3D skull models. The final implant design should be verified by neurosurgeons using 3D printed models.

Interventions

DEVICE3D deep learning neural network system

With the consent of the patient, we will assist in the production of images of 3D defect blocks for free (3D deep learning neural network system (3D DNN) system process planning), complete the repair and reconstruction under the clinical routine surgery, and track the repair results after surgery. meet medical needs.

Sponsors

Ministry of Science and Technology, Taiwan
CollaboratorOTHER_GOV
Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Scheduled for cranioplasty 2. Informed consent

Exclusion criteria

(1)No informed consent

Design outcomes

Primary

MeasureTime frameDescription
Number of patients where there is no need to adapt the Patient Specific Implant (PSI) edges6 weeks after surgery by standardised questionnaireNumber of patients where there is no need to adapt the Patient Specific Implant (PSI) edges
Number of patients where there is no need to augment/fill clefts between the Patient Specific Implant (PSI) and patient´s bone6 weeks after surgery by standardised questionnaireNumber of patients where there is no need to augment/fill clefts between the Patient Specific Implant (PSI) and patient´s bone

Countries

Taiwan

Contacts

Primary ContactYau-zen chang
zen@mail.cgu.edu.tw(03)211-8800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026