NCT06714747 Soft Tissue Prediction in Orthognathic Surgery by Making Anatomically Accurate Virtual Model
| NCT ID | NCT06714747 |
| Status | Recruiting |
| Phase | — |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna |
| Condition | Orthognathic Surgery |
| Study Type | OBSERVATIONAL |
| Enrollment | 10 participants |
| Start Date | 2022-01-11 |
| Primary Completion | 2026-09-11 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 10 participants in total. It began in 2022-01-11 with a primary completion date of 2026-09-11.
⚠ 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
The role of orthognathic surgery in the correction of dento-skeletal dysmorphies, whether they are Class II or Class III or asymmetries, is to improve both the function and aesthetic appearance of thepatient. Both aspects are equally important to achieve optimal results. When the surgeon plans the surgery, he or she must therefore take into account the effects that bone displacements will have at the level of the soft tissues directly involved in the surgery, such as the maxilla and mandible. Traditionally, such surgery consists of an orthodontic presurgical phase1,2 .
Eligibility Criteria
Inclusion Criteria: * Patients undergoing orthognathic surgery and preoperative radiographic study with CBCT and MRI * Patients with age \> or = 18 years old * Obtaining informed consent * Patients with preoperative teleradiography and orthopantomography Exclusion Criteria: * patients with cleft lip-palate, facial malformations and/or syndromes (syndromes with involvement of the cephalic extremity, such as sd of Apert. Cropuzon, Ofeiffer, Treacher Collins) * patients who have undergone application of Medpor prostheses or who have undergone ancillary procedures (lipofilling, fillers, volumetric facial augmentations with insertion of polyethylene ketone prostheses)
Contact & Investigator
Claudio Marchetti, MD
PRINCIPAL INVESTIGATOR
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Frequently Asked Questions
Who can join the NCT06714747 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Orthognathic Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06714747 currently recruiting?
Yes, NCT06714747 is actively recruiting participants. Contact the research team at claudio.marchetti@aosp.bo.it for enrollment information.
Where is the NCT06714747 trial being conducted?
This trial is being conducted at Bologna, Italy.
Who is sponsoring the NCT06714747 clinical trial?
NCT06714747 is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. The principal investigator is Claudio Marchetti, MD at IRCCS Azienda Ospedaliero-Universitaria di Bologna. The trial plans to enroll 10 participants.