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Dental grinding secrets revealed: study measures each stroke on tough zirconia crowns

NCT ID NCT07280130

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
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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 Results may not be published yet.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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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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

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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This status has not been confirmed recently, so it may be out of date.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 study aims to find out how much tooth-replacement material is removed with each grinding stroke when adjusting a zirconia crown. Researchers will have 120 participants—dental students, interns, and experienced clinicians—grind standardized zirconia blocks and measure the material removed using a 3D scanner. The goal is to provide data that helps dentists adjust crowns more accurately, reducing guesswork and improving fit.

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 120 people

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

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

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

The study population consists of 120 participants from three levels of dental training and early clinical practice, recruited from a dental school and affiliated clinical institutions. The sample includes: 1. Fourth-year dental students 2. Sixth-year dental interns 3. Clinicians with 0-5 years of post-graduation experience Participants are generally healthy adults capable of performing fine motor tasks required for dental procedures. Exclusion criteria include acute hand/upper-limb injuries, neuromuscular disorders, uncorrected poor vision, and inability to follow a metronome rhythm.

Ages

20 to 40 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: Group A: Forty fourth-year dental students who have completed preclinical courses in operative dentistry, complete denture prosthodontics, and fixed prosthodontics (Part I). They have little to no experience in adjusting zirconia. Group B: Forty sixth-year dental interns. Each participant will be tested twice-once before and once near the end of their clinical training. A questionnaire will also record their prosthodontic clinical experience within the past year. Group C: Forty licensed clinicians with 0-5 years of post-graduation experience (with practical experience in zirconia adjustment). A questionnaire will also document their clinical experience in prosthodontics. Exclusion Criteria: * Acute upper-limb/hand injuries or postoperative recovery within the past 3 months that may affect grip strength or fine motor control. * Neuromuscular disorders or tremor/postural control impairments (e.g., essential tremor, peripheral neuropathy, moderate to severe carpal tunnel syndrome) that prevent stable operation. * Uncorrected or inadequately corrected vision that does not meet the requirements for close-range tasks (e.g., inability to clearly see fine markings at a distance of 30-40 cm even with correction). * Inability to follow the metronome rhythm (100 beats per minute).

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Conditions

The condition(s) this trial relates to.

Bites and Stings

As listed by the trial registrant

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How to take part

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