ClinicalTrials.gg
Not yet recruitingNCT07814794AugRealDentUpdated Sep 25, 2026

Augmented Reality Dentistry

An interventional study of Surgery and Patients requiring orthodontic treatment. in Edentulism, Malocclusion; Displaced Teeth and TEETH EXTRACTION, sponsored by University of Bari Aldo Moro. Not yet recruiting at 1 site in Italy. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by University of Bari Aldo Moro · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Sex
All
01

Study summary

This study aims to evaluate the accuracy of augmented reality (AR)-assisted dental procedures. Patient-specific anatomical data will be acquired using cone-beam computed tomography (CBCT) and intraoral scanning and integrated to create a three-dimensional virtual model for treatment planning. Different dental procedures, including tooth extractions, dental implant placement, and orthodontic procedures, will be virtually planned before treatment. During the clinical procedure, the planned anatomical and procedural information will be visualized through an AR system, providing real-time guidance to the operator. The accuracy of AR-assisted treatment will be assessed by comparing the preoperative virtual plan with the postoperative clinical outcome, evaluating deviations between planned and achieved results.

02

Conditions studied

  • Edentulism
  • Malocclusion; Displaced Teeth
  • TEETH EXTRACTION

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03

In context

Malocclusion

323 studies on the registry are indexed under Malocclusion; 85 are open to participants now.

This study's planned enrollment of 10 is below the median of 37 across 242 interventional studies indexed under Malocclusion.

Browse Malocclusion studies →

Lead sponsor

University of Bari Aldo Moro is the lead sponsor of 30 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

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.

Inclusion criteria

  • Good health according to the System of the American Society of Anesthesiology
  • Aged older than 18 years
  • No general medical for surgery or orthodontics

Exclusion criteria

Exclusion Criteria:

Smoking more than 15 cigarettes a day

  • Pregnancy
  • Acute infections
Terms in these criteria, in plain language(1)

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.

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.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    Patients requiring dental treatment

    Patients requiring dental treatment, including tooth extraction, dental implant placement, or orthodontic treatment, for whom CBCT imaging and intraoral scanning are clinically indicated and who are eligible for augmented reality-assisted treatment.

    Procedure: Surgery · Procedure: Patients requiring orthodontic treatment.

Interventions

  • ProcedureSurgery

    Performance of oral surgical procedures using augmented reality to visualize and identify anatomical landmarks.

  • ProcedurePatients requiring orthodontic treatment.

    Dental and oral surgical procedures will be performed using augmented reality guidance, which provides real-time visualization of the preoperative treatment plan and relevant anatomical landmarks. AR guidance will be used to support procedures such as tooth extractions, dental implant placement, and orthodontic treatments, allowing the operator to follow the virtually planned treatment during the clinical procedure.

06

What researchers measure

Primary outcomes

  1. Accuracy of Osteotomies and Odontotomies Assessed by Linear and Angular Deviation from the Preoperative Surgical Plan

    Postoperative imaging will be superimposed on the preoperative virtual surgical plan, and the deviation between the planned and achieved osteotomy/odontotomy will be quantified. Accuracy will be assessed using linear deviation, expressed in millimeters (mm), and, where applicable, angular deviation, expressed in degrees (°). Measurements will include the discrepancy in the position, extent, and orientation of the performed surgical cuts relative to the corresponding planned cuts. For each osteotomy or odontotomy, the measured deviations will be recorded and summarized using descriptive statistics, including mean, standard deviation, median, range, and 95% confidence intervals, as appropriate.

    Time frame: 1 month

  2. Accuracy of Freehand Three-Dimensional Orthodontic Bracket Positioning Assessed by Linear and Angular Deviations from the Planned Position

    The accuracy of freehand orthodontic bracket placement will be evaluated by comparing the clinically achieved bracket position with the predefined three-dimensional virtual bracket position. Digital models obtained after bracket placement will be superimposed on the corresponding preoperative digital models or virtual treatment plan. Three-dimensional discrepancies between the planned and achieved bracket positions will be quantified for each bracket. Accuracy will be assessed using linear deviations, expressed in millimeters (mm), along the mesiodistal, occlusogingival, and buccolingual axes, as well as angular deviations, expressed in degrees (°), including tip, torque, and rotational discrepancies. For each bracket, the measured deviations will be recorded and summarized using descriptive statistics, including mean, standard deviation, median, range, and 95% confidence intervals, as appropriate. Aggregate values may also be calculated at the patient and study-group levels.

    Time frame: 1 month

07

Study locations

1 site
08

References and documents

Publications

  • Thomas AA, Sivakumar A. An evaluation of the accuracy of bracket positioning with and without loupes using 3Shape Ortho Analyzer software. J Taibah Univ Med Sci. 2022 Sep 16;18(1):98-103. doi: 10.1016/j.jtumed.2022.08.010. eCollection 2023 Feb. PubMed 36398025 ↗
  • Kwon HB, Park YS, Han JS. Augmented reality in dentistry: a current perspective. Acta Odontol Scand. 2018 Oct;76(7):497-503. doi: 10.1080/00016357.2018.1441437. Epub 2018 Feb 21. PubMed 29465283 ↗
  • Strobele DA, Othman A, Meier MA, Aboulazm K, von See C. Augmented reality in orthodontics for bracket placement using conventional mobile devices: Technical note. J World Fed Orthod. 2023 Dec;12(6):280-283. doi: 10.1016/j.ejwf.2023.08.003. Epub 2023 Sep 13. PubMed 37709634 ↗
  • Macrì, M.; D'Albis, G.; D'Albis, V.; Timeo, S.; Festa, F. Augmented Reality-Assisted Surgical Exposure of an Impacted Tooth: A Pilot Study. Appl. Sci. 2023, 13, 11097. https://doi.org/10.3390/app131911097

Individual participant data

Plan to share: Undecided

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Oct 2026, 1 month later.

Of 153 non-industry interventional studies with no phase under Malocclusion, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 30. This study's planned 1 month is below that.

Counting every sponsor, half of 163 studies reached it within 19 months; a quarter within 10 and three quarters within 32.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 29, 2026
First posted
Sep 11, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Oct 1, 2026
CompletionEst.
Nov 1, 2026
Last update
Sep 25, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Site contacts
Changed at 1 site. See the sites
Show the site
  • University of Bari Aldo Moro · Bari, ItalyContact added (no phone or email listed)
Sep 25, 2026
Show all 1 update
  1. Sep 25, 2026
    Site contacts Changed at 1 site. See the sites
    Show the site
    • University of Bari Aldo Moro · Bari, ItalyContact added (no phone or email listed)

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07814794
Lead sponsor
University of Bari Aldo Moro
Collaborators
Minia University
Responsible party
Giuseppe D'Albis (Principal investigator, University of Bari Aldo Moro) — Principal investigator
First posted
Sep 11, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Oct 1, 2026 (estimated)
Completion
Nov 1, 2026 (estimated)
Last update
Sep 25, 2026

Study contacts

Giuseppe D'Albis, Dr.
Contact
giuseppe.dalbis@uniba.it
+393495103642
Mahmoud H. Raheel, Dr.
Contact
Mahmoud_rahel10@yahoo.com
+20 10 23090373
Giuseppe D'Albis, Dr
principal investigator · University of Bari Aldo Moro
Mahmoud H. Raheel, Dr.
principal investigator · Orthodontics Department of Minya University
Wael M. Refai, Prof.
study chair · Minia University
Saverio Capodiferro, Prof
study chair · University of Bari Aldo Moro
Kareem M. Gaber, Dr.
principal investigator · Minia University
Vincenzo D'Albis, Dr.
principal investigator · University "G. d'Annunzio" Chieti - Pescara
Michele D'Attilio, Prof.
study chair · University "G. d'Annunzio" Chieti - Pescara

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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