Automatic Registration of Digital Dental Model to CBCT ImageCBCTNCT04563117
Automatic Versus Semiautomatic Registration of Digital Dental Cast to Cone Beam Computed Tomography Image
An observational study of Automatic Registration of Digital Dental Model to CBCT Image, run by Cairo University.
Trial summary
An observational Cross-sectional Study to compare the accuracy and reliability of the automatic registration of digital dental model to CBCT image versus the semiautomatic point-based registration. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Automatic Registration of Digital Dental Model to CBCT Image
- How many people
- 10 participants
- Where
- No sites listed yet
- Study dates
- Jun 2021to 1 Jun 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Partially edentulous patients who will come to Oral and Maxillofacial Radiology department, Faculty Dentistry, Cairo University for CBCT imaging seeking implant treatment and fulfilling the inclusion criteria of the study will be considered as potentially eligible participants.
Who may be able to join
- Partially edentulous patient.
- Patients having a minimum of three teeth distributed through the jaw with clear and prominent anatomical landmarks that can be used for point-based registration.
Who cannot join
- Completely edentulous patient.
- Patients with pathological lesions or fracture in jaws.
- Presence of radiopaque restoration with a resultant CBCT artefact that could interfere with proper CBCT segmentation and accurate selection of points needed for point-based registration.
About this study
Official title: Accuracy of Automatic Versus Point-based Semiautomatic Registration for Superimposition of Digital Dental Cast to CBCT 3D Image in Computer Guided Planning: An Observational Study
An observational Cross-sectional Study to compare the accuracy and reliability of the automatic registration of digital dental model to CBCT image versus the semiautomatic point-based registration.
Read the detailed description
Settings:
Participants will be randomly selected from patients who will come to Oral and Maxillofacial Radiology department, Faculty of Dentistry, Cairo University for CBCT imaging for implant treatment.
Radiographic imaging of the patients by CBCT machine will be done at Oral and Maxillofacial Radiology Department, Faculty of Dentistry, Cairo University. While the steps of impression taking followed by stone dental cast pouring, then surface laser optical scanning of the patients' stone cast will be done at the Removable Prosthodontics Department, Faculty of Dentistry, Cairo University.
Variables:
The outcome of this study is accuracy and reliability of non-explored new registration technique (automatic registration) versus commonly used registration method (point-based registration).
Variables involved in this study includes: the CBCT image resolution, the accuracy of the surface optical scanner, the software used, the number of points used for registration (in point-based registration), the skills of the investigator who will carry out the registration procedures. To cancel the effect of these variables, Investigators are going to standardize the CBCT resolution, the surface optical scanner used, the software used in both registration techniques, the number of points used for point-based registration while regarding the investigator factor more than one will carry out the same procedures to assure the reliability and validity of the results.
Data sources and management:
- CBCT scanning: Each patient will be scanned by CBCT machine (Planmeca Promax 3D Mid - Asentajankatu, Helsinki, Finland) with a field of view that covers the entire jaw. Image will be exported and stored in DICOM (digital imaging and communication in medicine) format.
- Cast scanning: Dental cast will be obtained by taking impressions using alginate impression material and filling the impressions with plaster. The plaster cast will then be scanned by a 3D laser scanner to obtain digital image of the dental arch that will be exported and stored as STL (standard tessellation language) file.
- Image registration:
DICOM file of CBCT image and STL file of digital dental model will be imported to a dental 3D planning software (Blue Sky Plan, Blueskybio). Image registration of digital cast to CBCT images will be performed for each patient by two methods:
- Automatic registration After importing the STL (standard tessellation language) file of the digital model, direct registration function of the software will be used to automatically perform the registration process.
- Point-based registration Using point registration function of the software, three points will be selected at the same areas on the image of dental cast and CBCT image. Then, registration of both images will be automatically processed to finalize the superimposition of digital dental model to maxillofacial model. potential sources of bias:
- Investigators are going to standardize the CBCT resolution, the surface optical scanner used, the software used in both registration techniques, the number of points used for point-based registration.
- Registration will be performed by two oral radiologists independently; blinded from the results of each other.
- One of the radiologists will perform the registration twice with two weeks interval.
- Intra-observer and inter-observer will be evaluated to assure the reliability and validity of the results.
Study size:
investigators are planning a study of a continuous response variable from independent control and experimental subjects with 1 control(s) per experimental subject. In a previous study by Sang-Hoon in 2014 the response within each subject group was normally distributed with standard deviation 0.04. If the true difference in the experimental and control means is 0.07, investigators will need to study 12 subjects to be able to reject the null hypothesis that the population means of the experimental and control groups are equal with probability (power) 0.8. The Type I error probability associated with this test of this null hypothesis is 0.05.
Quantitative variables:
Handling of quantitative variables in the analyses The study involves two main groups; one for automatic registration and one for point based registration. Assessment of deviation in both groups will be made using a third party software and will be expressed in form of mean ± standard deviation in mm.
Statistical methods:
Data will be analysed using IBM SPSS advanced statistics (Statistical Package for Social Sciences), version 26 (SPSS Inc., Chicago, IL). Continuous data will be described using mean and standard deviation. Comparison between continuous data will be performed using t-test and ANOVA will be used to test interaction of variables. A p-value less than or equal to 0.05 will be considered statistically significant and all tests will be two tailed. Statistical power of the study will be set at 80 % with 95 % confidence level.
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Automatic registration | Not described | |
| Point-based registration | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Accuracy of registration.
Outcome Measured is the accuracy of registration, measuring tool is a third party software (Geomagic Control X) and measuring unit is millimeter (mm)
Measured: 2020- 2021
Secondary outcomes (1)
Inter and intra-observer reliability
Outcome Measured is Inter and intra-observer reliability, measuring tool is a Kappa test and measuring unit is K
Measured: 2020- 2021
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Sep 2020
- Study startJun 2021 (estimated)
- Primary completion1 Jan 2022 (estimated)
- Study completion1 Jun 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Automatic Registration of Digital Dental Model to CBCT ImageStudies of the same condition, open and under way.
- More trials run by Cairo UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 10 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Cairo University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Nada Said, Cairo University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04563117
- Sponsor's protocol ID
- ORAD 6-3-1
- Acronym
- CBCT
- Status last verified
- Feb 2021
- First submitted
- 14 Sep 2020
- Last updated
- 23 Feb 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 Feb 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Accuracy of Automatic Versus Point-based Semiautomatic Registration for Superimposition of Digital Dental Cast to CBCT 3D Image in Computer Guided Planning: An Observational Study
- ClinicalTrials.gov ID
- NCT04563117
- Acronym / sponsor ID
- CBCT / ORAD 6-3-1
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 10 participants (estimated)
- Lead sponsor
- Cairo UniversityUniversity, hospital or other
- Study start
- Jun 2021 (estimated)
- Primary completion
- 1 Jan 2022 (estimated)
- Study completion
- 1 Jun 2022 (estimated)
- First posted
- 24 Sep 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
An observational Cross-sectional Study to compare the accuracy and reliability of the automatic registration of digital dental model to CBCT image versus the semiautomatic point-based registration.
Detailed description
Settings:
Participants will be randomly selected from patients who will come to Oral and Maxillofacial Radiology department, Faculty of Dentistry, Cairo University for CBCT imaging for implant treatment.
Radiographic imaging of the patients by CBCT machine will be done at Oral and Maxillofacial Radiology Department, Faculty of Dentistry, Cairo University. While the steps of impression taking followed by stone dental cast pouring, then surface laser optical scanning of the patients' stone cast will be done at the Removable Prosthodontics Department, Faculty of Dentistry, Cairo University.
Variables:
The outcome of this study is accuracy and reliability of non-explored new registration technique (automatic registration) versus commonly used registration method (point-based registration).
Variables involved in this study includes: the CBCT image resolution, the accuracy of the surface optical scanner, the software used, the number of points used for registration (in point-based registration), the skills of the investigator who will carry out the registration procedures. To cancel the effect of these variables, Investigators are going to standardize the CBCT resolution, the surface optical scanner used, the software used in both registration techniques, the number of points used for point-based registration while regarding the investigator factor more than one will carry out the same procedures to assure the reliability and validity of the results.
Data sources and management:
- CBCT scanning: Each patient will be scanned by CBCT machine (Planmeca Promax 3D Mid - Asentajankatu, Helsinki, Finland) with a field of view that covers the entire jaw. Image will be exported and stored in DICOM (digital imaging and communication in medicine) format.
- Cast scanning: Dental cast will be obtained by taking impressions using alginate impression material and filling the impressions with plaster. The plaster cast will then be scanned by a 3D laser scanner to obtain digital image of the dental arch that will be exported and stored as STL (standard tessellation language) file.
- Image registration:
DICOM file of CBCT image and STL file of digital dental model will be imported to a dental 3D planning software (Blue Sky Plan, Blueskybio). Image registration of digital cast to CBCT images will be performed for each patient by two methods:
- Automatic registration After importing the STL (standard tessellation language) file of the digital model, direct registration function of the software will be used to automatically perform the registration process.
- Point-based registration Using point registration function of the software, three points will be selected at the same areas on the image of dental cast and CBCT image. Then, registration of both images will be automatically processed to finalize the superimposition of digital dental model to maxillofacial model. potential sources of bias:
- Investigators are going to standardize the CBCT resolution, the surface optical scanner used, the software used in both registration techniques, the number of points used for point-based registration.
- Registration will be performed by two oral radiologists independently; blinded from the results of each other.
- One of the radiologists will perform the registration twice with two weeks interval.
- Intra-observer and inter-observer will be evaluated to assure the reliability and validity of the results.
Study size:
investigators are planning a study of a continuous response variable from independent control and experimental subjects with 1 control(s) per experimental subject. In a previous study by Sang-Hoon in 2014 the response within each subject group was normally distributed with standard deviation 0.04. If the true difference in the experimental and control means is 0.07, investigators will need to study 12 subjects to be able to reject the null hypothesis that the population means of the experimental and control groups are equal with probability (power) 0.8. The Type I error probability associated with this test of this null hypothesis is 0.05.
Quantitative variables:
Handling of quantitative variables in the analyses The study involves two main groups; one for automatic registration and one for point based registration. Assessment of deviation in both groups will be made using a third party software and will be expressed in form of mean ± standard deviation in mm.
Statistical methods:
Data will be analysed using IBM SPSS advanced statistics (Statistical Package for Social Sciences), version 26 (SPSS Inc., Chicago, IL). Continuous data will be described using mean and standard deviation. Comparison between continuous data will be performed using t-test and ANOVA will be used to test interaction of variables. A p-value less than or equal to 0.05 will be considered statistically significant and all tests will be two tailed. Statistical power of the study will be set at 80 % with 95 % confidence level.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Automatic registration | – | – |
| Point-based registration | – | – |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Partially edentulous patients who will come to Oral and Maxillofacial Radiology department, Faculty Dentistry, Cairo University for CBCT imaging seeking implant treatment and fulfilling the inclusion criteria of the study will be considered as potentially eligible participants.
Key inclusion criteria (2 listed)
- Partially edentulous patient.
- Patients having a minimum of three teeth distributed through the jaw with clear and prominent anatomical landmarks that can be used for point-based registration.
Key exclusion criteria (3 listed)
- Completely edentulous patient.
- Patients with pathological lesions or fracture in jaws.
- Presence of radiopaque restoration with a resultant CBCT artefact that could interfere with proper CBCT segmentation and accurate selection of points needed for point-based registration.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Accuracy of registration.
Time frame: 2020- 2021
Outcome Measured is the accuracy of registration, measuring tool is a third party software (Geomagic Control X) and measuring unit is millimeter (mm)
1 secondary outcome
Inter and intra-observer reliability
Time frame: 2020- 2021
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Feb 2021.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Automatic Registration of Digital Dental Model to CBCT Image, run by Cairo University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 23 Feb 2021. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Accuracy of registration. (time frame: 2020- 2021). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Feb 2021; AzTrials last refreshed its copy on 7 Nov 2026.