Skip to content

VR Sedation in Third Molar Surgery

Sedation Sparing Effect of Virtual Reality in Third Molar Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04540666
Enrollment
40
Registered
2020-09-07
Start date
2020-09-01
Completion date
2024-09-30
Last updated
2023-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Keywords

Anaesthesia for dental surgery, Sedation for dental surgery

Brief summary

Anaesthesia or sedation for dental surgery is Challenging. Over-sedation, leading to upper airway obstruction, desaturation and apnoea, is very common. On the other hand, it is also very common that inadequate sedative drugs were given, leading to under-sedation with unsatisfactory experience during operation. Therefore, it is good if some other methods are provided for sedation, avoiding side effects associated with sedative drugs.

Detailed description

Immersive virtual reality (VR) is a form of distraction therapy and is believed to create an immersive experience that can restrict the mind from pain and anxiety and has been shown to be superior to simple distraction in reducing pain.

Interventions

DRUGPropofol

Targeted Controlled Propofol Infusion will be set at 1 micro gram/ml.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Unilateral impacted lower third molar that requires surgical removal * Depth of impaction within 8mm as measured by Winter's line. * Cantonese speaking

Exclusion criteria

* ASA \> III * BMI \> 35 * Known Obstructive Sleep Apnoea * Patients with known or potential difficult airway * Chronic use of sedatives and opioid * Alcohol or drug abuse * Visual and hearing impairments * Claustrophobia * Cognitive impairment * History of seizure

Design outcomes

Primary

MeasureTime frameDescription
Intraoperative propofol doseFrom the start of anaesthesia to the end of anaesthesia, up to 2 hours after the start of surgeryAmount of propofol required during surgery

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026