- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06726551
AI Recognition of Important Structures in Otolaryngological Surgery
December 5, 2024 updated by: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Developing a system for artificial intelligence to recognize anatomical landmarks in otolaryngological surgery, enabling real-time tracking of critical temporal bone structures during surgery.
Study Overview
Status
Recruiting
Detailed Description
Take the example of the Al recognition and prediction of the incus, external semicircular canal, facial nerve, and facial nerve recess.
Within the defined surgical area, annotated data points are utilized to identify and segment the incus and the lateral semicircular canal based on their relative positions and angles concerning the posterior wall of the external auditory canal and the surrounding tissues.
Detailed descriptions of the incus and lateral semicircular canal within the surgical area include: Incus: The incus is a small anvil-shaped bone located in the middle ear.
It connects to the malleus laterally and the stapes medially.
Identifying the incus accurately is crucial due to its proximity to the facial nerve and its involvement in the ossicular chain that transmits sound vibrations.
Lateral Semicircular Canal: This is one of the three semicircular canals in the inner ear, oriented horizontally.
It is involved in detecting rotational movements of the head.
Proper identification is necessary to avoid damaging the canal, which could result in vertigo or balance issues.
Input features include further contrast adjustment and localized magnification of images.
The enhanced images are classified and localized using the trained model, and the consistency of multiple frames is utilized to determine the final positions of the facial nerve and the facial recess.
Statistical analysis is conducted to predict the positions of the facial recess relative to the incus and lateral semicircular canal, providing reference information for surgeons.
The system continuously monitors changes in the surgical area, offering dynamic feedback and optimizing the model's accuracy and robustness through incremental training.
Study Type
Observational
Enrollment (Estimated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Haidi Doctor Yang
- Phone Number: +86-131 7882 1663
- Email: yanghd@mail.sysu.edu.cn
Study Contact Backup
- Name: Jiaqi Doctor Pang
- Phone Number: +86-135 1272 2134
- Email: pangjq3@mail.sysu.edu.cn
Study Locations
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Guangdong
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Guangzhou, Guangdong, China, 510120
- Recruiting
- Sun Yat-sen Memorial Hospital
-
Contact:
- Liushan Ou
- Phone Number: +86 20 8133 2587
- Email: oulsh@mail.sysu.edu.cn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
otolaryngological diseases requiring mastoidectomy
Description
Inclusion Criteria:
- Performing otolaryngological surgeries such as cochlear implantation, endolymphatic sac decompression, semicircular canal plugging, and acoustic neuroma surgery using a microscope.
- Microscopic exposure provides a comprehensive and clear view of the surgical area within the temporal bone.
Exclusion Criteria:
- No surgical video recording available.
- Unclear visualization of the surgical area during microscopic otolaryngological procedures.
- Incomplete visualization of the entire surgical process.
- Patients who did not undergo high-resolution temporal bone CT at our hospital or Shenzhen Deep Bay Hospital.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
otolaryngological diseases requiring mastoidectomy
Time Frame: 1 week from admission to discharge
|
|
1 week from admission to discharge
|
|
Relevant indicators to evaluate the accuracy of the model
Time Frame: From enrollment to the end of the study
|
|
From enrollment to the end of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Relevant indicators of other evaluation models
Time Frame: From enrollment to the end of the study
|
|
From enrollment to the end of the study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2020
Primary Completion (Estimated)
August 30, 2026
Study Completion (Estimated)
August 30, 2026
Study Registration Dates
First Submitted
November 27, 2024
First Submitted That Met QC Criteria
December 5, 2024
First Posted (Estimated)
December 10, 2024
Study Record Updates
Last Update Posted (Estimated)
December 10, 2024
Last Update Submitted That Met QC Criteria
December 5, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SYSKY-2024-529-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data cannot be made publicly available because they contain sensitive patient information and involved the current trade secrets and intellectual property rights of Guangzhou Hansi Medical Technology Co.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.