NCT06494709 Quantitative Evaluation of Attention to Faces After Orthognathic Surgery With Eye-tracking
| NCT ID | NCT06494709 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Centre Hospitalier Universitaire, Amiens |
| Condition | Dentofacial Deformities |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2024-07-02 |
| Primary Completion | 2026-07 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2024-07-02 with a primary completion date of 2026-07.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Dentofacial deformities refer to morphological anomalies of the jaws. Their development during growth determines the shape of the lower third of the face and the type of dental occlusion. A maxillo-mandibular dysmorphosis associates morphological modification of the face and anomaly of the occlusion. If these anomalies are most often hereditary, they also depend on acquired factors such as swallowing, breathing, sucking or phonation disorders. Angle's classification defines three classes of dental occlusion: class I, when the ratio between the maxillary and mandibular first molars is normal, class II when the upper molar is too far forward, and class III when it is too far back. Class II and III dysmorphoses can result in an alteration of the masticatory function, pain (TMJ, headaches) or sleep apnea. At the same time, they cause patients to experience a decrease in self-esteem, anxiety and social discomfort. Class II and II usually require orthodontic treatment and orthognathic surgery to correctly align the jaws. This surgery has a positive impact on the dental occlusion and the functions concerned, but also on the facial morphology, all of which often leads to an improvement in the patient's quality of life. Standardized photographs presenting control subjects (class I) and patients (class II and class III) before and after surgery will be included in an approximately 10 min video sequence. Naive participants will look at this sequence during which the faces of the controls and the patients - before and after surgery - will alternate, with the instruction being free visual exploration of the images. The total fixation durations in defined areas of interest (eyes, nose, mouth, chin) will be recorded with an eye tracking device and the results will be processed using a dedicated software.
Eligibility Criteria
Inclusion Criteria: * Naïve subject with regard to dentofacial deformities and their management * Subject with no known facial pathology * Subject having provided an informed consent * Subject \> 18 years old Exclusion Criteria: * Subject familiar with dentofacial deformities and their management (e.g., health professionals in the relevant specialties) * Subject with known facial pathology (dentofacial deformity or other) * Subject under guardianship, curators or justice protection
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06494709 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Dentofacial Deformities. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06494709 currently recruiting?
Yes, NCT06494709 is actively recruiting participants. Contact the research team at dakpe.stephanie@chu-amiens.fr for enrollment information.
Where is the NCT06494709 trial being conducted?
This trial is being conducted at Amiens, France.
Who is sponsoring the NCT06494709 clinical trial?
NCT06494709 is sponsored by Centre Hospitalier Universitaire, Amiens. The trial plans to enroll 60 participants.