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Digital smile makeover: new trial uses face scans to guide Full-Mouth rehab

NCT ID NCT07314034

Disease control Sponsor: Menoufia University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a fully digital method for full-mouth dental rehabilitation in 10 adults aged 20-45 with bite problems, missing teeth, or smile concerns. The approach uses 3D scans of the teeth, face, and jaw to plan treatment, which may include tooth movement, guided implant placement, and custom crowns or veneers. The goal is to restore proper bite function and improve smile appearance with precise, comfortable results.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Digital dental workflow including guided implant placement, TAD-assisted molar intrusion, and custom crowns/veneers
What this could lead to
If successful, this could offer a more accurate and efficient way to restore bite function and smile esthetics using digital planning.
What could go wrong
This is a very small early trial with only 10 participants, so results may not apply to everyone. Dental implants carry risks like infection or implant failure.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 10 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2024

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adult patients aged 20-45 years with partial or complete edentulism, bite dysfunction, or esthetic concerns requiring full-mouth rehabilitation. Participants must be medically fit for implant and minor orthodontic procedures, have adequate bone for implant placement or be candidates for TAD-assisted tooth movement, and be willing to undergo treatment using a fully digital, facially guided workflow. Both male and female patients capable of providing informed consent and complying with follow-up visits are eligible.

Ages

20 to 45 years

Sex

Anyone

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults aged 20-45 years with partial or complete edentulism requiring full-mouth rehabilitation. * Patients with bite dysfunction, malocclusion, or esthetic concerns suitable for digital workflow treatment. * Adequate bone volume for implant placement or candidates for TAD-assisted tooth movement. * Willingness to undergo treatment using a fully digital, facially guided workflow and comply with follow-up visits. * Ability to provide informed consent. Exclusion Criteria: * Systemic conditions contraindicating implant or surgical procedures (e.g., uncontrolled diabetes, immunosuppression). * Active oral infections or untreated periodontal disease. * Heavy smokers (\>10 cigarettes/day) or substance abuse. * History of head and neck radiation therapy or bisphosphonate use. * Pregnancy or breastfeeding. * Inability to comply with treatment or follow-up protocol.

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Conditions

The condition(s) this trial relates to.

anodontia Malocclusion

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Malocclusion

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Faculty of Dentistry

    RECRUITING

    Shibīn al Kawm, Menoufia, Egypt

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