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AI vs. doctor talk: which calms nerves before tooth surgery?

NCT ID NCT07019688

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 study looked at 105 adults getting a wisdom tooth removed under anesthesia. Researchers tested whether getting information verbally, through traditional materials, or from an AI source changed how anxious patients felt. The goal was to see which method helps people feel calmer and more aware of risks before the procedure.

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

105 people

The number who actually took part.

Started

Jun 2025

Finished

Feb 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.

Who is studied

The study population consists of adult patients aged 18 to 40 years who are scheduled for the extraction of impacted mandibular molar teeth with a predicted moderate level of difficulty and no anticipated complications. Eligible participants must be systemically healthy, not taking any regular medications, and must have no prior history of sedation, general anesthesia, or surgical removal of impacted molars. Individuals who have previously received verbal, written, or visual information regarding impacted molar extraction will be excluded. Only patients who voluntarily consent to participate and are agreeing to receive preoperative information will be included.

Ages

18 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: * Indication for moderately difficult, non-complicated impacted mandibular molar extraction * Aged 18-40 years * No systemic disease or regular medication use * No previous procedures under sedation or general anesthesia * No history of impacted molar surgery or complicated extractions * No prior verbal, written, or visual information on molar extractions Exclusion Criteria: * Complex or multiple (\>2) molar extractions * Intellectual disability * Emergency cases * Refusal to participate or to receive preoperative information

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Kırıkkale University, Faculty of Dentistry

    Kirikkale, Turkey (Türkiye)

More trials for these conditions

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