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Implementing Virtual Reality (VR) to Reduce Sedation

RecruitingNAAges 21 Years - 65 YearsAllNYU Langone Health
NCT06349564 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The study is a prospective pilot patients aged 21 to 65 undergoing screening colonoscopy or diagnostic upper endoscopy. Patients are administered minimal sedation (2 mg of Versed and 25 mg of Fentanyl) and are given Virtual Reality (VR) goggles to wear for the duration of the procedure. The purpose of this study is to assess the feasibility, effect, and safety of using VR goggles during endoscopic procedures to decrease sedation requirements, enhance patient satisfaction, and reduce recovery time.

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📋 Eligibility rules (as published)
INTERVENTION GROUP Inclusion Criteria: * Undergoing screening colonoscopy or diagnostic upper endoscopy for GERD or dyspepsia at NYU Langone Brooklyn Hospital * Aged 21 to 65 Exclusion Criteria: * Visual impairments such as blindness which would impair them from watching the entertainment videos. * Patients with history of CAD, * History of seizures, * History of vertigo, * History of allergy to plastic, * ASAII or III, * Patient with active GI bleed, having either melena or hematochezia. CONTROL GROUP Inclusion Criteria: * Underwent screening colonoscopy or diagnostic upper endoscopy for GERD or dyspepsia at NYU Langone Brooklyn Hospital * Aged 21 to 65 Exclusion Criteria: * Visual impairments such as blindness which would impair them from watching the entertainment videos * Patients with history of CAD * History of seizures * History of vertigo * History of allergy to plastic * ASAII or III * Patient with active GI bleed, having either melena or hematochezia
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What it tests

  • Pico 4 Enterprise headset with noise cancelling headphones
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Where

1 site
NYU Langone Brooklyn
Brooklyn, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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