Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Could a quick digital scan replace goopy molds for dentures?

NCT ID NCT07377890

Knowledge-focused Sponsor: Mohammed Bin Rashid University of Medicine and Health Sciences 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a digital intraoral scanner can capture the shape of the mouth as accurately as the traditional border-molded impression method for making complete dentures. Ten adults who have lost all their teeth will get both types of impressions, and researchers will compare the digital scans to the conventional ones for precision and consistency. The goal is to see if the faster, less messy digital approach could be a reliable alternative.

What this could mean

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

Active substance
intraoral scanning (digital impression) and conventional border-molded impression
What this could lead to
If successful, this could show that digital scanning is a reliable alternative to traditional messy impressions for making dentures, potentially improving comfort and convenience.
What could go wrong
This is a very small early study with only 10 participants, so results may not apply to everyone. It only measures accuracy, not long-term denture fit or patient satisfaction.

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

About 10 people

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

Started

Oct 2025

Expected to finish

Jun 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.

Ages

18 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Patients attending DDH for complete dental prosthesis. * Fully edentulous patients * All alveolar ridge classifications of Cawood and Howell 1988 (Cawood and Howell, 1988) * Above 18 years old * Arabic and English-speaking patients * Good physical health (ASA class 1 or 2) * Willing to provide informed consent. Exclusion Criteria: * Dentate patients * Implant-attachment-supported complete denture. * Patients un-willing to participate (non-consented patients) * Patients with severe gag reflex * Patients who are mentally unstable, drug users or alcoholics

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Complete dentures are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

anodontia

As listed by the trial registrant

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

Complete dentures Dental impression techniques Digital impression accuracy Edentulism

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

  • Dubai Dental Hospital

    RECRUITING

    Dubai, 505055, United Arab Emirates

More trials for these conditions

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