Can a VR headset replace the Dentist's drill of fear?
NCT ID NCT07738718
First seen Jul 31, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study tests whether wearing a virtual reality headset during dental procedures can reduce pain and anxiety compared to standard care. Adults needing similar fillings on both sides of their mouth will receive one side with VR distraction and the other without, allowing a direct comparison. Researchers will measure pain, anxiety, heart rate, and patient satisfaction to see if VR improves the dental experience.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual reality headset used as a distraction technique during dental treatment
- What this could lead to
- If effective, VR could become a drug-free way to ease pain and anxiety during routine dental care, improving patient comfort.
- What could go wrong
- The trial is small and early, so results may not apply broadly. VR may not work for everyone, and some people might find it uncomfortable.
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
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13 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Aug 2026
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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 (≥18 years) requiring bilateral Class I restorative dental treatment. * Presence of bilateral Class I carious lesions extending to the inner one-third of dentin (D3) with symptoms of reversible pulpitis. * Willing and able to provide written informed consent. * Willing to participate in the study and comply with study procedures. Exclusion Criteria: * Children (\<18 years). * American Society of Anesthesiologists (ASA) Physical Status Class III or higher. * Deep Class I carious lesions with pulpal involvement. * Mentally or medically compromised patients. * Patients presenting with acute dental pain, such as acute pulpitis.
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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
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Professor Muhammad Zubair Ahmad
Ar Rass, Al-Qassim Region, 58883, Saudi Arabia
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