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Digital showdown: which impression technique fits the resorbed jaw best?

NCT ID NCT07764640

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 14, 2026 · Last updated Aug 14, 2026

Summary

This study compares three common dental impression techniques for people with severely resorbed lower jaws who need complete dentures. Using 3D scanning and deviation analysis, researchers will measure which technique produces the most accurate final impression. The goal is to identify a method that could lead to better-fitting dentures and improved comfort for patients with significant bone loss.

What this could mean

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

Active substance
Three dental impression techniques: conventional (alginate and zinc oxide eugenol), wax, and compound, each followed by alginate.
What this could lead to
If one technique proves more accurate, it could improve the fit and comfort of dentures for people with severely resorbed lower jaws.
What could go wrong
This is a small study with only 8 participants, so results may not apply to everyone. The findings are about accuracy, not long-term denture success.

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

8 people

The number who actually took part.

Started

Dec 2024

Finished

Jun 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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: \- Exclusion Criteria:Inclusion Criteria: 1. Completely edentulous patients with severely resorbed mandibular ridges. 2. Patients requiring a mandibular complete denture. 3. Patients able to tolerate the impression procedures and attend the required study visits. 4. Patients willing to participate in the study and provide informed consent. Exclusion Criteria: 1. Patients with systemic or local conditions that contraindicate conventional dental impression procedures. 2. Patients with pathological lesions or significant abnormalities affecting the mandibular denture-bearing area. 3. Patients unable to tolerate or cooperate with the impression procedures. 4. Patients who decline to participate or withdraw their informed consent. -

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Faculty of Dentistry, Tanta University

    Tanta, Gharbia Governorate, Egypt