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AI-Assisted Facial Surgical Planning

Artificial Intelligence-Assisted Facial, Periocular, and Orbital Analysis and Surgical Planning

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04319055
Enrollment
17932
Registered
2020-03-24
Start date
2009-01-01
Completion date
2019-07-30
Last updated
2021-02-18

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

Conditions

Artificial Intelligence, Facial Plastic and Reconstructive Surgery, Orbital Diseases, Periocular Diseases

Keywords

Facial Plastic and Reconstructive Surgery, Periocular Diseases, Orbital Diseases, Artificial Intelligence

Brief summary

Computer vision using deep learning architecture is broadly used in auto-recognition. In the research, the deep learning model which is trained by categorized single-eye images is applied to achieve the good performance of the model in blepharoptosis auto-diagnosis.

Detailed description

This auto-diagnosis system of blepharoptosis using machine learning architecture will assist in telemedicine, such as early screening of childhood ptosis for prompt referral and treatment. People could use this software via mobile devices to get a primitive diagnosis before they reach the physicians. Furthermore, in primary health care, where there is no oculoplastic surgeon, the software could assist primary care physicians or general ophthalmologists, in identifying the need for a referral.

Interventions

None listed

Sponsors

Stanford University
CollaboratorOTHER
National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

\[Inclusion Criteria\] 1. The participants who were 20-year-old or above, 2. Surgical informed consent was endorsed by the participants themselves, 3. Participants who have surgical indications of the oculofacial surgeries, and 4. The participants who agreed on photograph taking after explanation by the surgeon at outpatient clinics. \[

Exclusion criteria

\] 1. The participants who were 19-year-old or under, 2. The participants who don't have surgical indications of the oculofacial surgeries, 3. The participants who were designed for minimal invasive treatments, such as Botox or any kind of fillers injection, 4. The participants who refused photograph taking for any reason, and 5. The participants who are not available for standard quality of photograph taking, such as bedridden patients.

Design outcomes

Primary

MeasureTime frameDescription
The model performance is evaluated by accuracyThrough study completion, an average of 1 yearAn Artificial Intelligence Approach
AUC (Area Under the Curve)Through study completion, an average of 1 yearAn Artificial Intelligence Approach
ROC (Receiver Operating Characteristics) curve.Through study completion, an average of 1 yearAn Artificial Intelligence Approach
An Artificial Intelligence Approach to Identifying Facial, Periocular, and Orbital DiseasesThrough study completion, an average of 1 yearThe model interpretability is accessed by Grad-CAM (Class Activation Maps).

Countries

Taiwan

Outcome results

None listed

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