A Phase 1/2 interventional study of face scanning pre and post orthognathic surgery in Mandibular Prognathism and Orthognathic Surgery, sponsored by Cairo University. Enrolling by invitation at 1 site in Egypt. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2024-12-09.
Sponsored by Cairo University · Phase 1/2, Interventional, and Diagnostic
Aim of study: To evaluate the accuracy of soft tissue prediction in orthognathic surgery using handheld scanners versus optical scanners.
Research hypothesis (null hypothesis): there is no difference in prediction accuracy between laser scans and handheld scans.
Primary objective: To evaluate The Accuracy of soft tissue prediction in orthognathic surgery using handheld scanner versus laser scanner
.
Secondary objective:
To evaluate scanning time, cost efficiency, and ease of use. patients will be treated from mandibular prognathism using only mandibular set back or bimaxillary surgery After six months postoperatively, 3D facial scans is obtained and exported to software to perform superimposition of the predicted and post operative results to assess the accuracy of soft tissue prediction By measuring the difference in millimeter between prespecified points
Aim of study: To evaluate The Accuracy of soft tissue prediction in orthognathic surgery using handheld scanner versus optical scanner.
Research hypothesis (null hypothesis) that there is no difference in prediction accuracy between laser scans and handheld scans.
Primary objective: To evaluate The Accuracy of soft tissue prediction in orthognathic surgery using handheld scanner versus laser scanner .
Secondary objective:
To evaluate scanning time, cost efficiency, ease of use. 8. Trial design
One group of patients will be assigned to this trial:
One group: same patient will be scanned by both devices preoperatively and post operatively.
Trial design: prospective clinical trial( diagnostic accuracy study )
III. Methods A) Participants, interventions \& outcomes 9. Study settings: Oral and Maxillofacial Surgery clinic, Faculty of Dentistry, Cairo University. 10. Eligibility criteria:
Inclusion criteria:
Exclusion criteria:
The surgical technique:
All surgeries will be carried out with endotracheal intubation under general anaesthesia.
Postoperative Management:
Suture will be removed after 7 days post operative.
Accuracy measurement:
After six months post operative 3d facial scans is obtained and exported to software to perform superimposition of the predicted and post operative results to assess the accuracy of soft tissue prediction By measuring the difference in millimeter between prespecified points
1-full face 2-subnasal 3-labrale superioris 4- labrale inferioris 5-pogonion 6- corners of the mouth Then the degree of accuracy will be measured in percentage
Follow up:
All patients will undergo CT scans before the first follow-up 3 days postoperative.
Strategies to improve adherence to intervention protocol:
Criteria for discounting allocated intervention Uncooperative patients are refusing treatment and follow up.
Side effects and the degree of risk and expected to occur and how to deal with them Any temporary or permanent adverse effect will be recorded, documented, and treated including (facial asymmetry, pain trismus, paranesthesia, edema, and infection, flap dehiscence and plate exposure).
In the event of temporary side effects such as swelling or numbness, the patient will be followed up periodically and the necessary medications will be prescribed to get rid of these symptoms.
If facial asymmetry occurs after the operation, the necessary corrective measures will be taken, such as following up with the orthodontist or repeating the surgical procedure if necessary.
the event of a bacterial infection, the patient will be given the necessary medications after examination and confirmation of the source and cause of the infection and plate removal if needed
For patients equal to and less than 21 years old, a written consent should be obtained from their parents or guardian that they understand the treatment plan and agree for their children to undergo the surgical procedure and they understand the harms and side effects of this procedure and they will adhere to the follow up plans.
Outcome name Measuring Device Measuring Unit Primary
Soft tissue prediction accuracy
Computer Software Difference between prespecified measuring points in mm 1-full face 2-subnasal 3-labrale superioris 4- labrale inferioris 5-pogonion 6-corners of the mouth
Then turned into percentage Secondary scanning time Stopwatch seconds
Ease of use
scale Score from 1-10
1 very easy 10 very hard Cost efficiency Cost price pounds
Visit 5: six months postoperative clinical follow up and post operative soft tissue scanning.
Time Procedure Visit 1 Day 0 Case evaluation and diagnosis, request CT scan and soft tissue scan.
Visit 2 Week 1 Patient education, consent signing, anesthesiologist consultation.
Visit 3 Week 2 Surgical procedure. Visit 4 Week 3 First follow up, questionnaire,
Visit 5 Week 26 postoperative CT scan evaluation and soft tissue scanning and suture removal.
57 studies on the registry are indexed under Malocclusion, Angle Class III; 11 are open to participants now.
This study's planned enrollment of 11 is below the median of 32 across 53 interventional studies indexed under Malocclusion, Angle Class III.
Browse Malocclusion, Angle Class III studies →Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.
Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.
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Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Patients with facial mandibular prognathism that requires orthognathic surgery.
Exclusion Criteria:
Dental malocclusion that could be treated with orthodontic treatment only.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraindication
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
same patient will be scanned twice using both devices the optical face scanner and the handheld optical scanner
Procedure: face scanning pre and post orthognathic surgery
patient will be scanned pre operative using both scanners and then undergo orthognathic surgery then will be rescanned again 6 montsh later
soft tissue prediction accurace
3d facial scans is obtained and exported to software to perform superimposition of the predicted and post operative results to assess the accuracy of soft tissue prediction By measuring the difference in millimeter between prespecified points 1-full face 2-subnasal 3-labrale superioris 4- labrale inferioris 5-pogonion 6- corners of the mouth Then the degree of accuracy will be measured in percentage
Time frame: six months after surgery
Plan to share: Yes
Supporting information: Study protocol, Statistical analysis plan, Informed consent form
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Malocclusion, Angle Class III →