Assessment of the Artifical Intelligence Assisted Registration Versus Conventional Point Based Registration on Cone Beam-computed Tomography (CBCT) With Heavy Metal Artifacts

NCT ID: NCT06273332

Last Updated: 2024-02-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-20

Study Completion Date

2024-02-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Our study investigates the accuracy and duration needed for 3D model registration using artifical intelligence (AI) assistance compared to conventional point-based registration. Manual segmentation of all cone beam computed tomography (CBCT) scans will be performed before the registration procedure.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

CBCT images and intraoral scans will be screened following specific eligibility criteria. 16 CBCT images and intraoral scans that will meet the inclusion criteria will undergo manual segmentation via 3D medical image processing software. Afterward, point-based registration and AI-assisted registration will be performed by a single operator using specialized implant planning software. Then, the registration accuracy will be examined by measuring the distances between the three-dimensional models of CBCT data and intraoral scans. Also, the duration required for registration will be calibrated and recorded by a stopwatch.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Registration Accuracy

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

AI-assisted registration

3D model registration will be carried out using artificial intelligence

Group Type EXPERIMENTAL

AI-assisted registration

Intervention Type OTHER

We will use artificial intelligence to register 3d model on intra-oral scan

Point-based registration

3D model registration will be carried out using point-based approach

Group Type ACTIVE_COMPARATOR

Point-based registration

Intervention Type OTHER

We will use five references points or more to perform model registration

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

AI-assisted registration

We will use artificial intelligence to register 3d model on intra-oral scan

Intervention Type OTHER

Point-based registration

We will use five references points or more to perform model registration

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

CBCT scans for either the maxilla or mandible or both and intraoral scans or manual impressions with metal restorations.

Exclusion Criteria

Scans without metal restorations.
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Nehal Ibrahim Ahmed Shobair

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Private maxillofacial digital lab

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AI surgery protocol

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.