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Oral Surgery Virtual Reality Glasses Study

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Jul 2026 → Dec 2026
See other at-risk trials from Boston University

Record History

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  1. Minor Primary and study completion pushed from Jul 2026 to Dec 2026v10
  2. Minor Primary and study completion dates: Mar 2026 to Jul 2026v9
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Nov 2025 to Nov 18, 2025
    • Site details revised
    v8
  4. Notable Start date: Sep 2025 to Nov 2025
    • Primary and study completion dates: Dec 2025 to Mar 2026
    v7
  5. Minor Start date: Aug 2025 to Sep 2025v6
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  1. Notable Start date: Jun 2025 to Aug 2025v5
  2. Notable Start date: Mar 2025 to Jun 2025
    • Primary and study completion dates: Sep 2025 to Dec 2025
    v4
  3. Minor Primary and study completion dates: Jun 2025 to Sep 2025
    • Start date: Jan 2025 to Mar 2025
    v3
  4. Notable Primary endpoints revised (6)v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
3,263 trials monitored
See 159 trials at risk
The goal of this randomized trial is to investigate if using virtual reality (VR) glasses for patients who require non-emergent oral surgery procedures under intravenous (IV) sedation improves their overall experience compared to using standard of care safety glasses. This study has two primary objectives. 1. To evaluate if VR glasses can improve patient tolerance during IV access, sedation induction, and the surgical procedure. 2. To investigate whether the use of VR glasses reduces the amount of sedation required for induction and throughout the oral surgery procedure. 80 subjects will be randomly assigned 1:1 to either wear VR glasses playing a relaxing video and audio or VR glasses that will only serve as eye protection (control group).
Trial Details
NCT Number NCT06723158
Lead Sponsor Boston University
Conditions
(from sponsor)
Procedural Anxiety, Procedural Pain
Related terms Generalized Anxiety Disorder, Procedural Pain
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov