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Mandibular PrognathismPhase 1/2NCT06724497

Evaluating the Accuracy of Soft Tissue Prediction in Patients With Mandibular Prognathism After Orthognathic Surgery Using Handheld Scanner Versus Optical Scanner A Prospective Clinical Trial

A Phase 1/2 study testing face scanning pre and post orthognathic surgery in people with Mandibular Prognathism and Orthognathic Surgery, run by Cairo University at 1 site in Egypt.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 50 years
Conditions the study is for
Mandibular Prognathism, Orthognathic Surgery
What is being tested?
face scanning pre and post orthognathic surgery
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
11 participants
Where
1 siteEgypt
Study dates
24 Sep 2024to 24 Sep 2025
Phase
Phase 1/2
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • • Patients with facial mandibular prognathism that requires orthognathic surgery.
  • Age (18- 50 years).
  • Patients are willing for the surgical procedure and follow-up, with informed consent

Who cannot join

  • • Dental malocclusion that could be treated with orthodontic treatment only.
  • Patients with contraindications for general anesthesia.
  • Patient on radiotherapy.
  • Patients suffer from bone disease

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Egypt1 site
  • Faculty of Dentistry

    Cairo, Giza Governorate, 35855

Other trials in Egypt

About this study

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.

Read more

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

Read the detailed description

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:

  • Patients with facial mandibular prognathism that requires orthognathic surgery.
  • Age (18- 50years).
  • Patients are willing for the surgical procedure and follow-up, with informed consent (appendix 1).

Exclusion criteria:

  • Dental malocclusion that could be treated with orthodontic treatment only.
  • Patients with contraindications for general anesthesia.
  • Patient on radiotherapy.
  • Patients suffer from bone disease. 11. Interventions Preoperative Investigations
  • From the point of eligibility for general anesthesia, complete blood picture, body weight, urine albumin, blood glucose level, kidney and liver function.
  • Administration of peri-operative antibiotics.
  • A multi-slice CT scan will be demanded in a form of DICOM files ( Digital Imaging and Communications in Medicine) for proper diagnosis and confirmation of patient compatibility to the eligibility criteria and digital planning of the study group.
  • For each patient soft tissue scanning will be taken using cr-scan ferret scanner (Creality,shinzen,china) file will be imported to specialized software PROPLAN CMF™ (Leuven, Belgium)
  • then soft tissue scan will be done using optical scanner then the file will be imported to a specialized software PROPLAN CMF™ (Leuven, Belgium)
  • for segmentation process and superimposition of the soft tissue scan and the CT dicom file and planning the osteotome and fabrication of surgical guide for accurate positioning and fixation of bone segment.
  • Sterilization of the patient-specific plates and splints
  • For hemostasis an Epinephrine solution in dilution of 1:200.000 with lignocaine 0.5 mg\ml injected along lines of surgical incisions 5 min before the surgery.

The surgical technique:

All surgeries will be carried out with endotracheal intubation under general anaesthesia.

  1. the planned osteotomies are performed on the upper jaw (maxilla), lower jaw (mandible), or both, depending on the treatment plan.
  2. Repositioning of Jaw Bones: into the planned alignment to correct the underlying skeletal discrepancies. This may involve moving the jaws forward, backward, upward, or downward as needed to achieve proper facial harmony and function.
  3. Stabilization: using plates and screws to stabilize the bones in their new position. This promotes proper healing and ensures long-term stability of the surgical outcome.

Postoperative Management:

  • Postoperative instructions include a sleeping in a supine position semi-up righted, Strict oral hygiene measures.
  • Postoperative medications include prophylactic broad-spectrum antibiotics for 5 days' post operatively, nonsteroidal anti-inflammatory drug, diclofenac.

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:

  • The patient will be educated about the treatment protocol including a rationale for each step and an emphasis on the significance of follow-up appointments and home. Medicine.
  • All patients will be given reminder phone calls at the time of the predetermined follow updates.

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.

  1. Outcomes:

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

  • For standardization of follow up the accuracy of soft tissue prediction will be measured by superimposition the planning with the postoperative 3D scan of the patient Then, the distance between the planning and the scan will be estimated in millimeters. Then software will give a percentage
  • scanning time will be estimated in seconds.
  • Ease of use
  • cost 13. Participant timeline Patient will be treated in (5) visits . Visit 1: case evaluation and diagnosis, request CT scan and soft tissue scan. Visit 2: patient education, anesthesiologist consultation, consent signing. Visit 3: operation day. Visit 4: one week after surgery clinically evaluation and Patient questionnaire will be filled .

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.

Being tested
face scanning pre and post orthognathic surgery
Keywords
Prognathism, soft tissue prediction, face scanner, handheld scanner, optical scanner, orthognathic surgery, prediction accuracy
Medical subject headings
Malocclusion, Angle Class III, Prognathism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • face scanning pre and post orthognathic surgeryProcedure or surgery

    patient will be scanned pre operative using both scanners and then undergo orthognathic surgery then will be rescanned again 6 montsh later

Study groups in NCT06724497
Study groupRoleWhat they receive
patient with mandibular prognathismOthersame patient will be scanned twice using both devices the optical face scanner and the handheld optical scanner
Receives: Procedure: face scanning pre and post orthognathic surgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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

    Measured: six months after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Dec 2024
  2. Study start24 Sep 2024
  3. Primary completion24 Apr 2025 (estimated)
  4. Study completion24 Sep 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
11 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06724497
Sponsor's protocol ID
337
Status last verified
Dec 2024
First submitted
5 Dec 2024
Last updated
9 Dec 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing face scanning pre and post orthognathic surgery in people with Mandibular Prognathism and Orthognathic Surgery, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 9 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

soft tissue prediction accurace (time frame: six months after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Dec 2024; AzTrials last refreshed its copy on 6 Nov 2026.

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