Full-3D Computer-Assisted Workflow for the Diagnosis and Correction of Deformities? Dentofacial
NCT ID: NCT06806605
Last Updated: 2025-02-04
Study Results
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.
RECRUITING
50 participants
OBSERVATIONAL
2020-01-11
2026-11-11
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The nature of the dentofacial deformities was mainly related to skeletal discrepancies between the maxillae, such that the malocclusion could not be resolved by orthodontic treatment alone. The resolution of these conditions required a perfect synergy between orthodontic therapy (aimed at dental alignment of the individual arches) and surgical therapy (aimed at morphological harmonization of the face and obtaining the correct occlusion).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Application of a Simplified Method of Complete Denture Fabrication for Severely Resorbed Mandibular Ridges
NCT02339194
Effectiveness of the Single Implant-retained Mandibular Overdenture Treatment
NCT01801566
Anterior Mandibular Region for Immediate Implant Placement
NCT06527950
The Evaluation of Facial Bone Changes After Early Implant Placement Protocols "Clinically and Radiographically".
NCT06165913
Digital Obturators in Maxillectomy Cases
NCT06527053
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Orthognathic surgery allows the repositioning of the jaws in all three spatial planes. This procedure is indicated for patients with:
* Class 3 malocclusion, caused by maxillary retrusion, mandibular prognathism, or a combination of the two;
* Class 2 malocclusion, due to mandibular retrusion, with a normally conformed, protruded, or retruded maxilla and/or with excessive verticality;
* Class 1 malocclusion, characterized by consensual bimaxillary retrusion (a condition that may be seen in complex medical issues, such as in OSAS patients);
* Facial asymmetries caused by overgrowth on one side or facial torsion;
* Other malocclusions not correctable with orthodontic treatment alone, such as transversal or dento-alveolar deficits;
* Sequelae from facial trauma.
Orthognathic surgery has progressed rapidly since the 1950s when surgical techniques for treating most malocclusions that could not be resolved through orthodontics alone were first developed.
Subsequent technological advances have simplified the diagnosis of dentofacial deformities in three dimensions: Multislice CT (MSCT), Cone Beam CT (CBCT), Magnetic Resonance Imaging (MRI), stereophotogrammetry, dental arch scanning, software that allows surgical planning and outcome prediction, intraoperative navigation, and CAD-CAM technology. The conventional approach to orthognathic surgery (Orthodontic-first) consists of three phases: pre-surgical orthodontic treatment, the surgical phase, and post-surgical occlusion stabilization (post-surgical orthodontic treatment).
\*\*Orthognathic Surgery and Technology: From 2D Study to 3D\*\* To diagnose dentofacial deformities, the investigators have utilized 3D digital records created through dedicated software or devices. Real data and digital information are combined to simulate the surgical procedure.
\*\*3D Cephalometry\*\* Cephalometry is the method used to analyze the geometry of facial structures. Historically, this method was based on 2D radiology. The use of CT allowed the application of the same geometric criteria to 3D reconstructions of the skull and face. Studies assessing its accuracy showed that this method is comparable to standard 2D cephalometry for known measurements, but it adds a significant amount of new information, particularly regarding the rotational and translational aspects of the jaws and individual teeth.
\*\*3D Surgical Planning\*\* It is now possible to plan surgery using computer-assisted digital methods. The surgical plan can be transferred accurately to the patient through CAD-CAM-manufactured devices. The planning process can simulate both orthodontic and/or surgical treatment.
At the University of Bologna, the investigators have extensive experience with intraoperative navigation guided by 3D virtual simulation, combining navigation and virtual 3D surgery. they also have expertise in producing individualized CAD-CAM synthesis devices. It has been previously demonstrated that virtual orthodontic planning is as reliable as traditional methods using plaster models in orthodontic-only patients.
In fact, incorporating digital orthodontic planning into the orthodontic/surgical workflow is of great importance for the following reasons:
1. Initial treatment prediction to better guide therapeutic choices;
2. Improved communication between orthodontists and surgeons;
3. Enhanced communication with patients, providing an accurate prediction of the treatment plan from the beginning.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
T0 Initial 3D study
T0: the patient has not yet started orthodontic-surgical treatment and is carrying out the initial documentation collection;
3d analisys
To analyze the orthodontic-surgical set-up carried out as part of the normal care pathway of patients operated since January 2015 and who completed treatment on May 30, 2020 in the Orthodontic First patient.
T1 Preoperative 3D study
T1: the patient one month before surgery who collects the preoperative documentation;
3d analisys
To analyze the orthodontic-surgical set-up carried out as part of the normal care pathway of patients operated since January 2015 and who completed treatment on May 30, 2020 in the Orthodontic First patient.
T2 Final 3D study
T2: the patient has completed the orthodontic-surgical treatment and performs the collection of the final documentation. It is carried out within 12 months of the intervention.
3d analisys
To analyze the orthodontic-surgical set-up carried out as part of the normal care pathway of patients operated since January 2015 and who completed treatment on May 30, 2020 in the Orthodontic First patient.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
3d analisys
To analyze the orthodontic-surgical set-up carried out as part of the normal care pathway of patients operated since January 2015 and who completed treatment on May 30, 2020 in the Orthodontic First patient.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients undergoing orthognathic surgery.
* Patients between 18 and 60 years of age at the time of orthognathic surgery.
* Patients with dentoskeletal dysmorphia.
* Patients undergoing orthognathic surgery.
* Patients between 18 and 60 years of age at the time of orthognathic surgery.
* Obtaining informed consent.
Exclusion Criteria
* Patients who have not followed the data collection phases foreseen in the 3D Study.
18 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
IRCCS Azienda Ospedaliero-Universitaria di Bologna
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Claudio Marchetti, MD
Role: PRINCIPAL_INVESTIGATOR
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
IRCCS - Azienda Ospedaliero Universitaria di Bologna
Bologna, Emilia-Romagna, Italy
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FULL-3D OS
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.