Faculty of Dentistry
Cairo, Giza Governorate, 35855, Egypt
NCT Number: NCT06724497
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
Interested in participating?
Request Info18 year–50 year
All sexes
Interventional
Phase 1 / Phase 2
Cairo, Giza Governorate, 35855, Egypt
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
patient will be scanned pre operative using both scanners and then undergo orthognathic surgery then will be rescanned again 6 montsh later
Time frame: six months after surgery
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
Cairo University
Other
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