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Digital smile makeover: new implant workflow aims for perfect fit

NCT ID NCT07369583

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This completed study tested a fully digital, motion-integrated workflow for placing dental implants in people with no teeth. Twenty adults received implants in both jaws using special protocols (M-4 in the upper jaw, All-on-4 in the lower jaw). The approach used 3D scans and real-time jaw movement data to design custom-fit, one-piece zirconia teeth. The goal was to see if this digital method leads to stable bone levels around the implants.

What this could mean

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

Active substance
Monolithic zirconia dental prostheses placed using a motion-integrated digital workflow
What this could lead to
If successful, this approach could make full-arch dental implant procedures more precise and personalized, potentially improving fit and long-term outcomes.
What could go wrong
This is a small, completed study with only 20 participants and no control group, so results may not apply to everyone. Long-term success depends on individual healing and bone health.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

20 people

The number who actually took part.

Started

Jan 2024

Finished

Jan 2026

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.

Ages

40 months to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 40-65 years with edentulism in one or both arches. * Adequate bone volume in the anterior maxilla for M-4 protocol and mandible for All-on-4 placement. * Willingness to undergo full-arch implant rehabilitation using a digital workflow. * Ability to provide informed consent and comply with study procedures. Exclusion Criteria: * Systemic conditions contraindicating implant surgery (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.

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Conditions

The condition(s) this trial relates to.

Jaw, Edentulous

As listed by the trial registrant

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

Contacts and locations

Locations

  • Faculty of Dentistry

    Shibīn al Kawm, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.