CClinicalTrials.gg
Not yet recruitingNCT07112417"AR-MSP"Updated Aug 8, 2025

"Augmented Reality-Assisted Miniscrew Placement in Orthodontics: A Clinical Trial"

An interventional study of Augmented Reality and Conventional screw placement in Orthodontic, sponsored by Al-Azhar University. Not yet recruiting at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2025-08-08.

Sponsored by Al-Azhar University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Randomized
Sex
All
01

Study summary

This study aims to evaluate the effectiveness and accuracy of using Augmented Reality (AR) technology in the placement of mini-screws (Temporary Anchorage Devices) during orthodontic treatment. By combining CBCT images with digital dental scans and visualizing them using AR, clinicians can place mini-screws more precisely. The study is a pilot clinical trial involving patients at the Faculty of Dentistry, Al-Azhar University - Assiut Branch.

Read the detailed description

This is a pilot clinical trial designed to assess the feasibility and accuracy of augmented reality (AR)-guided mini-screw insertion in orthodontic patients. The study involves the use of CBCT imaging and digital intraoral scanning to create a 3D model of the patient's jaw. This model is then processed and integrated into an AR platform that allows real-time visualization of the ideal screw insertion site.

Participants are selected based on inclusion and exclusion criteria. After obtaining informed consent, CBCT and intraoral scans are performed. The proposed mini-screw location is determined digitally and projected using an AR device (tablet or headset) during the clinical procedure.

After insertion, a follow-up CBCT scan is taken to evaluate the deviation between the planned and actual screw positions (linear and angular deviation). Data on insertion time, patient comfort, and operator satisfaction will also be recorded.

The study is conducted at the Faculty of Dentistry, Al-Azhar University - Assiut Branch, with prior ethical approval obtained from the institutional review board.

02

Conditions studied

  • Orthodontic

Keywords

  • Augmented Reality
03

In context

Lead sponsor

Al-Azhar University is the lead sponsor of 505 studies on the registry; 167 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

Inclusion criteria

  • 1. Patients indicated for orthodontic mini-screw placement as part of their treatment plan.

    2. Age between 15 and 40 years.

    3. Good general health (ASA I or II).

    4. Adequate oral hygiene and healthy periodontal condition.

    5. Ability to understand and provide informed consent (or guardian consent for minors).

Exclusion criteria

Exclusion Criteria:

  • 1 . Systemic conditions affecting bone healing (e.g., uncontrolled diabetes, osteoporosis).

    2. History of craniofacial trauma, surgery, or congenital anomalies in the maxillofacial region.

    3. Ongoing periodontal disease or poor oral hygiene.

    4. Pregnancy or lactation.

    5. Use of medications influencing bone metabolism (e.g., bisphosphonates, corticosteroids).

    6. Allergy to local anesthetics or materials used in the procedure.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Active comparator
    Augmented Reality-Guided Mini-Screw Placement

    Participants in this group will undergo mini-screw placement using augmented reality (AR) guidance to enhance accuracy and reduce placement errors

    Device: Augmented Reality

  • Active comparator
    conventional Mini-Screw Placement

    Participants in this group will undergo mini-screw placement using conventional placement

    Procedure: Conventional screw placement

Interventions

  • DeviceAugmented Reality

    Participants in this group will undergo mini-screw placement assisted by augmented reality (AR) technology. A customized AR system will guide the clinician in real-time to ensure optimal screw positioning, improve accuracy, and minimize placement errors.

  • ProcedureConventional screw placement

    Participants in this group will receive mini-screw placement using the conventional freehand method without augmented reality assistance. The screws will be placed according to standard clinical protocols based on anatomical landmarks and clinician experience

06

What researchers measure

Primary outcomes

  1. Accuracy of screw placement

    Accuracy will be assessed using CBCT imaging compared to planned position

    Time frame: 1 week post-op

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — NO plan to share

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07112417
Lead sponsor
Al-Azhar University
Responsible party
omar hassan abd el azeem (studient of master, Al-Azhar University) — Principal investigator
First posted
Aug 8, 2025
Start date
Aug 31, 2025 (estimated)
Primary completion
Dec 1, 2025 (estimated)
Completion
Dec 1, 2025 (estimated)
Last update
Aug 8, 2025

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion